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In the present paper, we apply a blind fitting algorithm to model two-dimensional energy-incidence angle maps of soft x-ray resonant reflectivity measured in nanoscale epitaxial multilayers of multiferroic ε-Fe2O3 grown by pulsed laser deposition. The possibility of fitting the spectral shape of the complex refraction index across the Fe L3 absorption edge without having an initial guess about the optical constants has been demonstrated. The spectral shape fitting of the real (f1) and imaginary (f2) parts of the atomic scattering factor has been carried out by using a specially designed software utilizing OpenCL fast calculations on graphical processing units. The Kramers-Kronig relations between f1 and f2 are automatically taken into account by the fitting algorithm. A reasonable agreement between blindly generated and reference scattering factor spectra derived independently from an x-ray absorption spectroscopy experiment has been demonstrated. The blind fitting has been compared with the alternative refinement routines, in which small free variations of the reference spectral shapes (or no variations at all) have been allowed. The presented approach to the resonant x-ray reflectometry modeling makes it unnecessary to acquire the optical constant spectral shapes in advance and, thus, is especially helpful when such spectra cannot be physically measured, e.g., for a buried layer of a multilayer system. [ABSTRACT FROM AUTHOR]

The continuous phase transition phenomena and mechanism of pellets in the hydrogen blast furnace is achieved by dissecting the 40m3 hydrogen blast furnace. The results of the dissection reveal that the lumpy zone extends to the bosh of the hydrogen blast furnace (HBF), while it ends at about 2/3 of the stack in traditional blast furnace. The iron oxide (FeO x) began to appear in the upper stack, while the iron started to appear in the lower stack. The reduction rate and metallization rate at the bosh are measured at 95.18% and 95.54%. The content of ferrous oxide (FeO) decreases significantly (measured at 1.73% at the bosh), resulting in an increase in the melting point of the primary slag and a deterioration of its fluidity. FeO x formed in the upper stack continuously diffuses and merges into the gangue, which affects the subsequent transformation of FeO x. FeO x shows a preference for interacting with SiO 2 , CaO, and MgO, directly influencing the formation of slag in the cohesive zone. These findings offer valuable insights for numerical simulation and research on hydrogen-rich operation. • A 40 m3 experimental hydrogen-rich blast furnace is dissected. • The lumpy zone of hydrogen blast furnace extends to bosh. • The reduction rate and metallization rate at the bosh are 95.18% and 95.54%. • FeO x tends to react with SiO 2 to form high melting point substance. • A mechanism of iron and gangue transformation is proposed. [ABSTRACT FROM AUTHOR]

Selective oxidation is one of the primary methods used to synthesize high‐value‐added oxygen‐containing organic compounds from alkenes. In particular, the selective oxidation of natural cinnamaldehyde has gained prominence as one of the main routes to produce natural benzaldehyde, which is in short supply in the global spice market. In this study, FeSBA catalysts were synthesized by supporting Fe2O3 onto the surface of spherical SBA‐15 using pore‐induced deposition for the selective oxidation of cinnamaldehyde to benzaldehyde. The Fe2O3 supporting increased the specific surface area of SBA‐15 by approximately eightfold and significantly improved the utilization efficiency of the reaction sites on Fe2O3. Additionally, the formation of Fe−O−Si bonds by Fe2O3 and SBA‐15 promoted the generation of weak‐acidic sites on the catalyst surface, significantly increasing the oxygen‐physisorption capacity of Fe2O3. Furthermore, quenching experiments confirmed the generation of significant amounts of O2− and singlet‐oxygen species on the FeSBA surface. Theoretical calculations confirmed that the physisorption and chemisorption of cinnamaldehyde and oxygen, respectively, on the FeSBA surface promoted the formation of a tetrameric intermediate. These results contribute significantly to research on the selective oxidation theory of α,β‐unsaturated aldehydes to aldehydes using oxygen and could guide future studies aimed at elucidating and improving the process. [ABSTRACT FROM AUTHOR]

In this study, Au/α‐Fe2O3 sensing material was synthesized and used as the working electrode for dopamine sensing. The Au/α‐Fe2O3 composites were prepared with various loadings (0.5 %, 1 %, and 3 %) to enhance their sensing properties. All three composites were tested for dopamine sensing, with 1 % Au/α‐Fe2O3 showing the best response. The Au/α‐Fe2O3 composites were characterized using XRD, TEM, and SEM to confirm successful doping of Au on the iron oxide surface. The CV plot obtained by plotting Cyclic Voltammetry (CV) vs. dopamine (DA) was linear (R2=0.9872) for DA concentrations ranging from 6.25 μM–200 μM on 1 % Au/α‐Fe2O3. Similarly, the DPV plot between DPV vs. DA was linear (R2=0.9895) for the same DA concentration range on 1 % Au/α‐Fe2O3, with a detection limit of 0.19 μM. Interference and stability experiments were conducted with dopamine (DA), ascorbic acid (AA), and uric acid (UA). The results showed that DA sensing was not affected by the other two substances for up to 14 days. The signal results indicated that the current intensity remained at 90.75 % of the original, proving that this material has good stability. [ABSTRACT FROM AUTHOR]

Using Ambient Pressure X-ray Photoelectron Spectroscopy (APXPS), this study investigates the reduction behavior of iron oxides in direct reduction (DRI) and blast furnace (BF) pellets. H 2 , CO, and a H 2 –CO mixture are used as reducing agents at 650 °C. The investigation aimed to elucidate variations in the rate of reduction over time and under different conditions. Additionally, contour plots are generated to visualize the X-ray photoelectron peak intensity variations as a function of time. Furthermore, phase stability diagrams based on Fe– O –C and Fe– O –H systems are employed to enhance the understanding of reduction behavior. Results revealed that an increased gas flow rate significantly accelerated the reduction rate due to enhanced gas diffusion, while elevated pressure facilitated the reduction of wüstite to metallic iron. Notably, the DRI pellet achieves around 90% metallization degree reduction with hydrogen, but the introduction of carbon monoxide into the reducing gas prevented the reduction of the DRI pellet. In the case of BF pellet reduction, approximately 20% metallization degree is observed using H 2 –CO (50:50), yet subsequent reoxidation of the reduced iron to wüstite and magnetite occurred. Further investigation identified a significant increase in the partial pressure of H 2 O and CO 2 , particularly within the surface porosities, as the underlying cause of this reoxidation phenomenon. • APXPS used to study iron oxide surface reduction in DRI and BF pellets. • Increased gas flow rate and pressure accelerated reduction rate. • DRI pellet achieved ∼90% metallization with H 2 , however, the value was ∼9% for BF. • BF pellet attained ∼20% metallization with H 2 –CO, while DRI showed no reduction. • Using CO–H 2 , reoxidation observed in BF due to a rise in H 2 O–CO 2 partial pressure. [ABSTRACT FROM AUTHOR]

Conversion‐type anode materials with high theoretical capacities play a pivotal role in developing future aqueous rechargeable batteries (ARBs). However, their sustainable applications have long been impeded by the poor cycling stability and sluggish redox kinetics. Here we show that confining conversion chemistry in intercalation host could overcome the above challenges. Using sodium titanates as a model intercalation host, an integrated layered anode material of iron oxide hydroxide‐pillared titanate (FeNTO) is demonstrated. The conversion reaction is spatially and kinetically confined within sub‐nano interlayer, enabling superlow redox polarization (ca. 4–6 times reduced), ultralong lifespan (up to 8700 cycles) and excellent rate performance. Notably, the charge compensation of interlayer via universal cation intercalation into host endows FeNTO with the capability of operating well in a broad range of aqueous electrolytes (Li+, Na+, K+, Mg2+, Ca2+, etc.). We further demonstrate the large‐scale synthesis of FeNTO thin film and powder, and rational design of quasi‐solid‐state high‐voltage ARB pouch cells powering wearable electronics against extreme mechanical abuse. This work demonstrates a powerful confinement means to access disruptive electrode materials for next‐generation energy devices. [ABSTRACT FROM AUTHOR]

In this study, forming limit diagrams (FLDs), fracture toughness (FT), mechanical, magnetic, and electro-physical properties of Al/Fe2O3 composites have been investigated experimentally. Accumulative-roll-bonding (ARB) process was used to manufacture composite samples. Then, Al/Fe2O3 composites have been produced at 300∘C up to eight ARB passes. Also, magnetic composites have been fabricated with 0, 5% and 10wt.% of particles. The interlayer bonding quality was improved at higher passes. By studying the SEM rapture morphology, it was shown that the rapture mode changed to shear ductile for samples with more passes. For composite samples fabricated at higher passes and in comparison with the annealed sample, elongated dimples were turned to shallow dimples. FLDs area as the main forming criterion dropped severely after pass one and then began to improve at higher passes. Fracture test results showed that after the 8th pass, the value of FT improved gradually to the maximum value of 34.3MPam1∕2. [ABSTRACT FROM AUTHOR]

In this study, poly(n-isopropylacrylamide) (PNIPA) has been synthesized by the free-radical polymerization method using azobisisobutyronitrile the initiator. Then, nanoparticle-PNIPA composite is prepared with magnetic iron oxide (Fe3O4) nanoparticles synthesized by co-precipitation. The thermal decomposition kinetics of synthesized PNIPA and nanocoated PNIPA have been investigated. It has been observed that nanocoated PNIPA has a more stable structure at high temperatures than synthesized PNIPA. In the newly improved model equations relate to thermal decomposition kinetics, a special solution has been made with the new approach. Moreover, the calculated activation energies of the samples have been evaluated with response surface methodology (RSM). The ratios required to synthesize nanocoated-PNIPA under the optimum conditions have been determined by RSM. The activation energy of the nanocomposite obtains when 0.3170 g PNIPA is coated with 0.048 g Fe3O4 nanoparticle is determined as 127.757 kJ/mol. In other words, nanocoating has been increased the thermal stability of the synthesized composite. Poly (n-isopropylacrylamide) has been synthesized by free radical polymerization The Fe-O stretching vibration proves the existence of nanoparticle in FTIR spectra The thermal decomposition kinetics of synthesized PNIPA and Fe3O4-PNIPA nanocomposite have been evaluated by RSM. Magnetic nanoparticle reinforcement enhances the thermal stability of PNIPA [ABSTRACT FROM AUTHOR]

To achieve a coating density meeting the solid oxide fuel cell (SOFC) electrolyte requirements of high gas tightness and ionic conductivity, in this study, a new interface healing densification process based on a liquid-phase sintering induction mechanism was conducted on plasma-sprayed 8 mol% Y 2 O 3 -stabilized ZrO 2 (8YSZ) coatings. Using Fe 2 O 3 and Bi 2 O 3 as healing additives, metallurgical healing of unbound interfaces was achieved by impregnating the additives into the gap interfaces, followed by liquid-phase sintering at 1200 and 1050 °C. After healing, the YSZ coating exhibited a dense bulk-like microstructure with a significant reduction in the gas leakage rate by two orders of magnitude, and the oxygen ion conductivity of the coating was significantly increased. The YSZ coating healed with the Fe 2 O 3 additive showed an oxygen ionic conductivity nearly one order of magnitude higher than that of the as-sprayed coating, reaching more than 80% of the value of the high-temperature-sintered YSZ bulk. • A new interface healing process based on liquid-phase sintering was conducted on APS YSZ coatings. • The interface-healed YSZ coating exhibited a dense bulk-like microstructure. • The gas leakage rate of the interface-healed YSZ coating decreased by two orders of magnitude. • Ionic conductivity of the interface-healed YSZ coating reached > 80% of the sintered bulk. • The cell assembled with interface-healed YSZ-Fe 2 O 3 electrolyte achieved MPD of 1.04 W/cm2 at 800 °C. [ABSTRACT FROM AUTHOR]

This paper explores the important impact of Fe 2 O 3 on the synthesis, structure, hardness, and radiation shielding characteristics of Apatite–Wollastonite (AW) glass ceramics for bone implantation and shielding application. The prepared studied samples were prepared and the effects of Fe 2 O 3 addition on the synthesis process, density, and different physical and structural parameters comprehensively investigated. Additionally, the radiation shielding properties were determined by using PHITS simulation code and XCOM calculations for all samples. The results reveal that there is a significant impact of Fe 2 O 3 addition on density, hardness, and radiation shielding of AW glass ceramics. The Vickers hardness values were calculated as 547, 598, and 621 Hv in measurements under 0.1 kg load., the density values are found to be as 2.87, 3.07 and 3.28 g/cm3 for AW, Aw -1Fe, and Aw -2Fe, respectively. The highest linear attenuation coefficient in the AW- 2Fe is 0.096 cm−1, Aw -1Fe showed 0.084 cm−1 and AW gave 0.072 cm−1 at 6 MeV. This study underscores the pivotal role of Fe 2 O 3 as a multifaceted modifier in tailoring the properties of AW glass ceramics for bone implantation and other diverse applications extending from medical imaging to radiation and charged ions shielding. [ABSTRACT FROM AUTHOR]

This study investigated the effects of using ferric oxide nanoparticles (FO) and C2–C4 alcohols with diesel/biodiesel blend in a diesel engine. Optimum operating conditions were explored, and an engine speed of 1750 rpm was optimal. The concentration of FO was estimated to be 760 ppm, considering the best conditions for carbon nanotube (CNT) production. Ethanol was immiscible in diesel fuel; however, any biodiesel percentage in the blend made it miscible. The used engine was too small to run with a blend containing more than 3 % ethanol. Propanol and butanol were blended at the same ethanol concentration for comparative purposes. A blend with 30 % biodiesel (B30) was found to be the best diesel/biodiesel blend. This was detected by the best coefficient of variation (COV) with reasonable performance and emissions. Ferric oxide nanoparticles reduced COV and improved engine performance. The COV increased for tested alcohols. However, blending B30 with alcohols, especially butanol, improved thermal efficiency. FO and alcohol increased NOx emissions and decreased both CO and smoke opacity. They increased the peak pressure and the heat release rate while reducing the combustion duration. Nonetheless, no CNT traces were detected in the present study under any conditions. [ABSTRACT FROM AUTHOR]

Iron emissions from human activities, such as oil combustion and smelting, affect the Earth's climate and marine ecosystems. These emissions are difficult to quantify accurately due to a lack of observations, particularly in remote ocean regions. In this study, we used long‐term, near‐source observations in areas with a dominance of anthropogenic iron emissions in various parts of the world to better estimate the total amount of anthropogenic iron emissions. We also used a statistical source apportionment method to identify the anthropogenic components and their sub‐sources from bulk aerosol observations in the United States. We find that the estimates of anthropogenic iron emissions are within a factor of 3 in most regions compared to previous inventory estimates. Under‐ or overestimation varied by region and depended on the number of sites, interannual variability, and the statistical filter choice. Smelting‐related iron emissions are overestimated by a factor of 1.5 in East Asia compared to previous estimates. More long‐term iron observations and the consideration of the influence of dust and wildfires could help reduce the uncertainty in anthropogenic iron emissions estimates. Plain Language Summary: Human activities, such as smelting and oil combustion, release smoke and particles into the atmosphere. These particles often contain iron, which not only absorbs sunlight, contributing to atmospheric warming, but also serves as a nutrient for phytoplankton in various ocean regions. However, the precise extent of human‐induced iron emissions remains uncertain due to a lack of comprehensive monitoring data. In this study, we leverage a global data set of iron observations to refine our estimates of iron emissions attributed to human activities. Additionally, we examine other co‐released substances, such as carbon and nickel, to identify specific emission sources of iron. We employ statistical techniques to distinguish human‐caused iron emissions from those originating from natural sources like dust and wildfires. Moreover, we utilize iron oxide observations to constrain emissions originating from East Asia and Norway, which are estimated to originate largely from smelting emissions. Through the analysis of long‐term data sets, we provide lower and upper bounds to human‐caused iron emissions. Furthermore, we investigate the impact of reduced observation numbers and a sparse network on the range of estimated iron emissions. Our findings highlight the critical role of observation quality in accurately assessing iron emissions from human activities. Key Points: Anthropogenic total iron emissions are constrained to a factor of 3 in most global regions using long‐term aerosol observationsThe number of sites, interannual variability, and site selection filter can affect the model‐observation comparison uncertainty by 15%–50%Smelting‐related emissions are constrained to a factor of 1.5 using iron oxide observations from East Asia [ABSTRACT FROM AUTHOR]

AbstractInhalation exposure to iron oxide occurs in many workplaces and respirable aerosols occur during thermal processes (e.g. welding, casting) or during abrasion of iron and steel products (e.g. cutting, grinding, machining, polishing, sanding) or during handling of iron oxide pigments. There is limited evidence of adverse effects in humans specifically linked to inhalation of iron oxides. This contrasts to oxides of other metals used to alloy or for coating of steel and iron of which several have been classified as being hazardous by international and national agencies. Such metal oxides are often present in the air at workplaces. In general, iron oxides might therefore be regarded as low-toxicity, low-solubility (LTLS) particles, and are often considered to be nontoxic even if very high and prolonged inhalation exposures might result in diseases. In animal studies, such exposures lead to cancer, fibrosis and other diseases. Our hypothesis was that pulmonary-workplace exposure during manufacture and handling of SPION preparations might be harmful. We therefore conducted a systematic review of the relevant literature to understand how iron oxides deposited in the lung are related to acute and subchronic pulmonary inflammation. We included one human and several in vivo animal studies published up to February 2023. We found 25 relevant studies that were useful for deriving occupational exposure limits (OEL) for iron oxides based on an inflammatory reaction. Our review of the scientific literature indicates that lowering of health-based occupational exposure limits might be considered. [ABSTRACT FROM AUTHOR]

Introduction: Altrenogest (ALT) is widely used to regulate the estrous cycle of sows and mares; however, currently used oral solutions of ALT are deficient in terms of dose accuracy and stability during use. To resolve these problems, we aimed to prepare softgel capsules of ALT with a unit dose equal to the clinically administered dose. Method: The shell of the softgel capsule was mainly composed of gelatin and glycerol, with titanium dioxide and red iron oxide as masking agents. Using the shake flask method, the contents were screened for ethyl acetate as a lipophilic solubilizing carrier based on soya bean oil. The contents were automatically filled and compressed into softgel capsules by a softgel capsule machine. The quality of the prepared softgel capsules was evaluated through a drug content test, an in vitro release test, and stability studies. Furthermore, bioequivalence studies were conducted with atrenogest oral solution. Results: The content is an ALT concentration of 2% oil solution and the specification of the softgel is 20mg/capsule. In in vitro dissolution experiments, the softgel capsules were rapidly disintegrated and released in three different pH buffers, with a cumulative release rate of nearly 100% at 1 h. The softgel capsules were stable at high temperature and under strong light for 10 days, and the concentration of ALT was >99% in the 6-month accelerated and long-term tests. In the bioequivalence study, Tmax of the softgel capsules was 2.20 ± 0.77 h, t1/2 was 6.36 ± 1.74 h, and Cmax was 64.65 ± 20.69 ng/ml. The main pharmacokinetic parameters Tmax, Cmax, AUC0-t, and AUC0-8, did not differ significantly between the softgel capsules and the commercially available ALT oral solution (P > 0.05), and bioequivalence was demonstrated within the 90% confidence interval. Conclusion: The prepared softgel capsules have the advantages of higher content, ease of use with accurate dosing, good stability, and equivalence to ALT oral solution, implying that our softgels are ready for clinical use. [ABSTRACT FROM AUTHOR]

This review paper highlights the current toxicological aspects of magnetic nanomaterials in the field of medicine and the environment, conducted through a comprehensive literature review. The main goal was to investigate and analyze the key challenges identified in the literature that enhance the effective utilization of these systems, particularly focusing on magnetic iron oxide (Fe3O4) nanoparticles. We aimed to investigate the factors that influence their intended applications. We sought to understand how the characteristics of the produced NPs could be enhanced to improve their biocompatibility compared to existing samples in the literature. Moreover, we investigated morphological aspects intricately connected to physicochemical characteristics and their prospective applications in biomedicine. Additionally, we assessed the regulatory implications of nanostructured materials. Therefore, the initial aspect of this review delved into the historical evolution of nanoparticles, investigating significant milestones that have influenced the exploration of this technology. We examined the main discoveries, factors influencing the choice of synthesis methods, and the most prevalent approaches for surface functionalization employed by scientists for materials possessing superparamagnetic characteristics, such as iron oxide. The second aspect of the review focused on a survey-based exploration of the global regulation progress concerning superparamagnetic nanoparticles throughout the years. Additionally, we identified the main challenges encountered in establishing safety criteria for the diverse applications under investigation. This encompassed an assessment of the potential impacts of these materials on both human health and the environment. [ABSTRACT FROM AUTHOR]

The high-temperature oxidation behavior of Cr-Mn-Si alloyed steel by Fe 2 O 3 contained mold flux in high temperatures, and its effect on microstructure evolution were investigated in detail by TEM, EBSD, CLSM, SEM, and XPS. A novel oxidation mechanism was firstly revealed that the Fe 2 O 3 in mold flux melts during high temperatures plays a role of oxidizing alloyed steels by the released free oxygen ions (O2−) from the transformation of Fe 2 O 3 (Fe3+) to FeO (Fe2+). The formed oxidized dots within the oxide layer changed from SiO 2 and MnSiO 3 to MnCr 2 O 4 spinel phases by increasing the content of Fe 2 O 3 in the mold flux. Notably, the amorphous SiO 2 was discovered in the core region of MnSiO 3 phase due to its selective oxidative behavior in high temperatures. This research provides conclusive evidence that the small size MnSiO 3 oxides can be acted as a nucleation core for the refinement of austenite grains through in-situ observation. [ABSTRACT FROM AUTHOR]

By incorporating the dual ceramic elements TiB 2 /B 4 C, we investigated their impact on the mechanical properties, thermal properties, and friction performance of copper-based powder metallurgy materials, and elucidated the friction wear mechanism. Additionally, machine learning algorithms were employed to predict the friction coefficient and stability coefficient. The conclusions are as follows:With the increase in the TiB 2 /B 4 C ratio, the trend of mechanical properties initially increases and then decreases, with the optimum ratio being 5:3 for TiB 2 and B 4 C, exhibiting superior mechanical properties. Moreover, B 4 C enhances the thermal conductivity of copper-based friction materials more effectively than TiB 2. In terms of overall friction performance, the ratio of TiB 2 to B 4 C at 5:3 yields better frictional properties. The primary components of the friction surface friction film are CuO, Cu 2 O, Fe 2 O 3 , and B 2 O 3 , transitioning from a ceramic film to a metallic film as the TiB 2 /B 4 C ratio increases. The friction wear mechanism shifts from abrasive wear to severe fatigue wear as the TiB 2 /B 4 C ratio increases, accompanied by oxidative wear. Furthermore, an AdaBoost algorithm model was developed to effectively predict the friction coefficient and stability coefficient, with accuracies of 0.9993 and 0.8739, respectively. [ABSTRACT FROM AUTHOR]

In this work, we demonstrate systematic studies on the influence of Fe 2 O 3 on the structural and optical properties of transparent B 2 O 3 –TeO 2 –Na 2 O glasses containing the different concentrations of Fe 2 O 3. The glasses were prepared via the standard melt quenching method, and the prepared glasses were characterized using, XRD, electron paramagnetic resonance (EPR), FTIR, and UV–visible spectroscopic techniques. Furthermore, we evaluated several physical properties of the glasses, including densities, molar volume, boron-boron separation, and oxygen packing density, with respect to the concentration of Fe 2 O 3 in the host glass matrix. It is observed that the density of the glasses and the average boron-boron distance found increase with Fe 2 O 3 concentration due to the modification in the glass network induced by the dopant ions. EPR spectra reveals the presence resonance signals at g ∼2.04 and g ∼4.26, hence it proves the existence of Fe3+ in distorted octahedral coordination and supported by UV–Vis absorption bands. The FTIR spectra revealed an increase in spectral intensity with the concentration of Fe 2 O 3. This was attributed to the formation of non-bridging oxygens through converting BO 4 units into BO 3 units, which Fe 2 O 3 mediated. The UV–visible spectral analysis showed a decreased energy band gap from 2.26 to 1.51 eV with increased Fe 2 O 3 concentration. Additionally, we determined the Urbach energy, refractive index, optical basicity, and electronegativity, which are presented in detail. [ABSTRACT FROM AUTHOR]

Oxidative degradation of chloramphenicol (CAP) using a hybrid approach (US/HA+/n-Fe2O3/SPC) involving sodium percarbonate (SPC; "solid H2O2" carrier), Fe2O3 nanoparticles (n-Fe2O3; H2O2 decomposition catalyst), hydroxylamine in its protonated form (HA+; Fe (III) to Fe (II) reducer), and ultrasonic cavitation (to increase the generation of hydroxyl radicals) has been studied for the first time. The average size of n-Fe2O3 synthesized by the sonochemical method, as calculated according to the Debye–Scherrer equation, was ~ 18 nm. The maximum degradation degree of CAP (83.1%) and first-order oxidative degradation rate constant of CAP as 1.253 × 10–3 s−1 were achieved using the modified sono-Fenton process under the optimized conditions as the initial concentration of CAP – 50 mg/L, the molar ratio of CAP:HA+:n-Fe2O3:SPC of 1:100:100:100, pH as 3, the temperature as 318 K, the specific ultrasonic power as 53.3 W/L, and the treatment duration of 7200 s. In general, the efficiency and intensity of CAP degradation increased with a decrease in the pH value, an increase in the molar ratio of CAP:HA+:n-Fe2O3:SPC, a decrease in the initial concentration of CAP, an increase in temperature, and showed a minor change with the specific power of US. The synergistic coefficient for the combination of the US and the heterogeneous Fenton process was 17.9. The active participation of hydroxyl radicals in the oxidative degradation of CAP using the modified sono-Fenton process was confirmed by scavenging experiments performed using tert-butyl alcohol. The proposed process can be a promising direction in the remediation of pharmaceutical effluents with significant potential for commercial exploitation. [ABSTRACT FROM AUTHOR]

The evaluation of the adsorption capacity of amine‐functionalized silica coated iron oxide magnetic particles (Fe3O4/SiO2‐NH2) as a highly recyclable adsorbent for Congo Red (CR) and Eriochrome Black T (EBT) azo‐dyes from water is reported. The Fe3O4/SiO2‐NH2 were prepared by a simple co‐precipitation method of iron oxide (Fe3O4) nanoparticles followed by silica coating on oleic acid coated Fe3O4. A series of investigation was performed to assess the various experimental parameters like contact time (0–360 min), pH (3–10), stirring speed (0–500 rpm), adsorbent dosages (0.02–0.12 g) and initial concentrations (0.02–0.15 mg mL−1) of dyes. According to the Langmuir isotherm, the maximum adsorption capacities of CR and EBT on Fe3O4/SiO2‐NH2 particles were found to be 211.86 mg g−1 and 81.98 mg g−1, respectively. In comparison, the pseudo‐second order model provided adsorption capacities of 200.40 mg g−1 for CR and 80.91 mg g−1 for EBT. Additionally, the maximum adsorption amounts of CR and EBT on Fe3O4/SiO2‐NH2 particles were 179.37 mg g−1 and 75.43 mg g−1, achieved within 300 min and 180 min at pH 3, respectively. The dye‐loaded particles were recoverable for CR and EBT removal by simple regeneration with 0.1 molL−1 NaOH solution to use the particles until more than five cycles. [ABSTRACT FROM AUTHOR]

The development of nanomaterials for dye degradation has garnered significant interest due to their efficiency, environmental benefits, and cost‐effectiveness. In this study, a nanocomposite adsorbent composed of α‐Fe2O3 coupled with carbon derived from eco‐friendly corn husk has been developed. This material effectively captured cationic dyes, Methylene Blue (MB) and Malachite Green (MG), from aqueous solutions, including industrial dye effluent from local industry. The synthesized nanocomposite demonstrated rapid removal of MB and MG from the solution without the need for additional oxidizing or reducing agents. The adsorption conditions by varying parameters such as adsorbent dose, contact time, solution pH, initial dye concentration, and temperature have been optimized. Adsorption isothermal studies indicated that the Langmuir isotherm model best explained the adsorption process. Kinetic studies revealed that the adsorption process follows a pseudo‐first‐order model for MB, while the intraparticle diffusion model is more appropriate for MG. Moreover, the nanocomposite exhibited excellent reusability and regenerability for dye adsorption. Our study showcases the effectiveness of the synthesized nanocomposite adsorbent, comprising α‐Fe2O3 integrated with carbon derived from eco‐friendly corn husk using a simple and sustainable methodology, in efficiently removing cationic dyes from textile wastewater. This approach offers a promising solution for environmental remediation. [ABSTRACT FROM AUTHOR]

A BiVO4/Fe2O3 heterojunction for non-enzymatic photoelectrochemical (PEC) determination of hydrogen sulfide (H2S) is reported. The BiVO4/Fe2O3 heterojunction promoted the separation of photo-generated carriers, reduced electron–hole recombination, and thus improved electron collection and photocurrent. The proposed BiVO4/Fe2O3/FTO sensor exhibited a linear range of 1–500 μM and a detection limit of 0.51 nM H2S. In addition, high selectivity, good reproducibility, and stability were obtained for H2S sensing. The detection of H2S in water and serum samples demonstrated its feasibility. This work provides a new strategy to detect and understand the bio-function of H2S in the biological environment. [ABSTRACT FROM AUTHOR]

This study focuses on the development of new amino-functionalized magnetic Fe2O3/SiO2 nanocomposites with varying silicate shell ratios (1:0.5, 1:1, and 1:2) for the efficient elimination of Hg2+ ions found in solutions. The Fe2O3/SiO2–NH2 adsorbents were characterized for their structural, surface, and magnetic properties using various techniques, including Fourier transform infrared spectrum (FT-IR), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Braunauer–Emmett–Teller (BET), thermogravimetric analysis (TGA), zeta-potential, and particle size measurement. We investigated the adsorption circumstances, such as pH, dosage of the adsorbent, and duration of adsorption. The pH value that yielded the best results was determined to be 5.0. The Fe2O3/SiO2–NH2 adsorbent with a silicate ratio of (1:2) exhibited the largest amount of adsorption capacity of 152.03 mg g−1. This can be attributed to its significantly large specific surface area of 100.1 m2 g−1, which surpasses that of other adsorbents. The adsorbent with amino functionalization demonstrated a strong affinity for Hg2+ ions due to the chemical interactions between the metal ions and the amino groups on the surface. The analysis of adsorption kinetics demonstrated that the adsorption outcomes adhere to the pseudo-second-order kinetic model. The study of adsorption isotherms revealed that the adsorption followed the Langmuir model, indicating that the adsorption of Hg2+ ions with the adsorbent occurred as a monomolecular layer adsorption process. Furthermore, the thermodynamic analyses revealed that the adsorption of Hg2+ ions using the adsorbent was characterized by a spontaneous and endothermic process. Additionally, the adsorbent has the ability to selectively extract mercury ions from a complex mixture of ions. The Fe2O3/SiO2–NH2 nanocomposite, which is loaded with metal, can be easily recovered from a water solution due to its magnetic properties. Moreover, it can be regenerated effortlessly through acid treatment. This study highlights the potential use of amino-functionalized Fe2O3/SiO2 magnetic nanoparticles as a highly efficient, reusable adsorbent for the removal of mercury ions from contaminated wastewater. [ABSTRACT FROM AUTHOR]

The ca. 480 Ma Albești granite (Southern Carpathians, Romania) is characterized by the presence of color zoned blue quartz grains, and is part of the rather extensive European Cambro-Ordovician blue quartz landscape. The color is heat sensitive, fading at temperatures as low as 300℃, inconsistent with the thermally stable, light scattering, nanometric rutile/ilmenite inclusions cited in literature. Extensive X- and Q-band electron paramagnetic resonance (EPR) investigations were carried out, searching for distinctive features of the Albești quartz that are directly or indirectly involved in the generation of the blue coloration. The analyzed quartz grains were extracted from three granite samples of varying coloration and anisotropy, and the quartz from each rock sample was further separated into colored and colorless fractions. The paramagnetic E' and [AlO4]0 centers, as well as Mn2+ ions localized in traces of amorphous associated minerals at grain boundaries or fissure planes, were observed in all quartz samples. Broad EPR lines associated with the presence of magnetic clusters were observed in the spectra of the white quartz sample and the corresponding colorless one. Isochronal annealing up to 500℃ induced the correlated recombination of the E' and [AlO4]0 centers, the strong decrease of the Mn2+ spectrum and the formation of a minority iron oxide phase at the grain boundaries and/or fissure planes. The EPR signature was similar for the colored and the corresponding colorless quartz samples, before and after annealing, showing that the heat sensitive coloration of the Albești quartz does not directly involve the presence of paramagnetic defects and/or minority magnetic phases. [ABSTRACT FROM AUTHOR]

This work includes the use of leaves of Mitragyna parvifolia for green synthesis of Fe 2 O 3 nanoparticles ( Fe 2 O 3 NPs), which offers a sustainable eco-friendly approach. Characterization of synthesized Fe 2 O 3 NPs was done by UV-visible, FTIR spectroscopy, XRD and FESEM studies. FTIR exhibited the existence of Fe-O, O–H and COO–Fe stretching owing to the occurrence of the carboxylic group. FESEM analysis revealed that the average size of Fe 2 O 3 NPs was 92 nm, which varies in their shape. The study also includes the determination of antibacterial, in vitro antioxidant and immunomodulatory efficacy of synthesized Fe 2 O 3 NPs. Results suggested that Fe 2 O 3 NPs exhibit potent antibacterial efficacy against B. subtilis and S. aureus, gram-positive as well as E. coli and P. aureginosa, gram-negative bacterial strains used in this study. The study exhibited significant (p < 0.01) in vitro antioxidant and immunomodulatory potential of synthesized Fe 2 O 3 NPs against concanavalin-A activated Wistar albino rat's splenocytes. The green synthesized Fe 2 O 3 NPs using M. parvifolia leaves may offer a novel approach in the medicinal and immunological field to overcome oxidative stress as well as enhance immune responses for potential health benefits of human beings. [ABSTRACT FROM AUTHOR]

The efficient graphene coated iron oxide (GCIO) nanoadsorbent was prepared for removal of various ions, viz., Cr(VI), Pb(II), and As(III), by coating graphene onto the iron oxide surfaces taken as a base material. The as-prepared nanoadsorbent was further characterized by several analytical techniques such as Fourier transform infrared (FTIR) spectroscopy, energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), Raman spectroscopy, Differential scanning calorimetry (DSC), and Zeta-potential measurements, respectively. These techniques provided valuable information about the nanoadsorbent and confirmed the interactions between Cr6+, Pb2+, and As3+ ions and the nanoadsorbent. The effect of concentration of adsorbate solution, contact time between adsorbate–adsorbent, and flow rate of adsorbate were studied using a sensitive, simple, and selective spectrophotometric method that enabled quantification of Cr6+, Pb+2, and As3+ ions, respectively. Various modeling of breakthrough curves was applied for monitoring progress of the adsorption process and the results showed that the three metal ions followed second order kinetic model thus confirming that GCIO is an excellent, effective, and economic adsorbent. [ABSTRACT FROM AUTHOR]

Predicting the liberation distribution of minerals in comminuted ore particles is one of the fundamental problems in mineral processing. However, there is still no widely accepted liberation model due to the complexity of the mineral fracture mechanism. In this study, the shape constants of the cumulative beta distribution were further optimized based on the investigation of the liberation distribution and fracture mechanism of iron oxide minerals in three types of iron ores with different grain sizes by locked-cycle grinding and batch grinding to model the liberation distribution of iron oxide minerals with different grinding methods. The results showed that the liberation distribution of iron oxide minerals in the three types of iron ores with locked-cycle grinding and batch grinding was related to intergranular fracture proportion and the closeness of ore particle size and mineral grain size. By relating the shape constants of cumulative beta distribution to ore particle size, mineral grain size, and the proportion of intergranular fracture, the developed liberation model well predicted the liberation distribution of iron oxide minerals with different grinding methods and its coefficient of determination (R2) was between 0.85–0.93. [ABSTRACT FROM AUTHOR]

Blue, green, and khaki spinels were produced by self-propagating high-temperature synthesis (SHS) using Co 3 O 4 –ZnO–Mg(NO 3) 2 ·6H 2 O–Al(OH) 3 –Al, Ni 2 O 3 –ZnO–Cr 2 O 3 –Al(OH) 3 –Al, and Co 2 O 3 –Fe 2 O 3 –Al(OH) 3 –Al mixtures. The composition of the synthesis products was characterized by X-ray diffraction and IR spectroscopy. The oxides Co 3 O 4 , Co 2 O 3 , ZnO, Ni 2 O 3 , Cr 2 O 3 , Fe 2 O 3 , and aluminum hydroxide Al(OH) 3 were used for the synthesis. Fuel was provided by aluminum powder (ASD-4). The spinel-type ceramic pigments were synthesized using layer-by-layer combustion, which involves two parallel exothermic reactions: aluminum oxidation and aluminothermic reactions. The fast self-propagating reactions and high synthesis temperatures rapidly destroy the structure of Al(OH) 3 hydroxide in the starting mixture, producing gaseous reaction products that prevent the sintering of the spinels. The surface morphology of pigment powders and their composition was studied using a Quanta 3D 200i, FEI Co. scanning electron microscope and a Philips SEM 515 scanning electron microscope equipped with a local energy dispersive X-ray analysis (EDAX). The particle size of the synthesized spinels was approximately 1–5 μm. Colored spinels powders obtained by the SHS process can be used as ceramic pigments. [ABSTRACT FROM AUTHOR]

The widespread industrial use of styrene highlights the urgent need for detecting and monitoring its harmful gases. The innovation of this study lies in synthesizing uniform Fe 2 O 3 nanoparticles using Ginkgo biloba and calcining them with CuOHF to prepare nanostructured materials, enhancing the performance of gas sensors. The effects of varying α-Fe 2 O 3 additions and calcination temperatures on the structure and gas-sensitive properties of the composites were systematically investigated. The results revealed that the optimal operating temperatures of the CuO–10%Fe 2 O 3 -400 sensor were reduced by 80 and 50 °C, and its response to 100 ppm styrene at 200 °C was significantly enhanced by 3.2-fold and 4.2-fold, respectively, compared to the single Fe 2 O 3 and CuOHF sensors. It is particularly noteworthy that the sensor exhibits excellent detection performance at a 50 ppb styrene concentration, with a response value of 1.2. The lamellar structure of CuOHF serves as a precursor for CuO, thereby increasing the surface area of the sensor in contact with the gas. During the calcination process, the released gases contribute to the formation of a porous structure, which together improves the adsorption capacity and stability of the sensor. Additionally, the heterojunction formed by the calcination of CuO (p-type) and Fe 2 O 3 (n-type) enhances charge transfer and increases gas adsorption capacity, highlighting its potential as a gas sensor. This composite material exhibits good sensitivity and reliability in monitoring hazardous gases like styrene, underscoring the significant value of this study in environmental monitoring and safety control. [ABSTRACT FROM AUTHOR]

The permeability of the Fe Soft Magnetic Composite (SMC) materials need further improve to broaden their application prospect. This research work presents a novel high permeability SMC material which has a low core loss (P cv). The Fe particles formed an elongated strip shape structure through the ball milling process, and the high permeability Mn 0.5 Zn 0.5 Fe 2 O 4 ferrite phase was formed around the elongated strip shape Fe particles via a high temperature in-situ reaction process (ZnO + MnO + Fe 2 O 3 –Mn 0.5 Zn 0.5 Fe 2 O 4). While the added high resistive SiO 2 phase aggregated at the long strip shape Fe particle outer surface and effectively increased the resistivity of the SMCs. As the percentage of the Mn 0.5 Zn 0.5 Fe 2 O 4 ferrite coating increase, the permeability of the double layer coated SMCs gradually increased from 38 for the 1 wt% Mn 0.5 Zn 0.5 Fe 2 O 4 coated SMCs to 170 for the 18 wt% Mn 0.5 Zn 0.5 Fe 2 O 4 coated SMCs. The 3 wt% Mn 0.5 Zn 0.5 Fe 2 O 4 coated SMCs has the lowest core loss (P cv) of 86.9 W/kg at 10 mT, 500 kHz. [ABSTRACT FROM AUTHOR]

Analyzing transition metal XPS peaks is widely used to determine surface composition and chemistry. However, these peaks have a complex structure, which is still the subject of investigation. Fe 2p analysis is a case in point where the multiplet structure and many-electron-effects lead to peak shapes that cannot be analyzed using standard approaches. Examination of the literature reveals that one of the most widely used approaches to data reduction when processing Fe 2p3/2 spectra involves using symmetric two- or three-component peak fitting with each peak effectively acting to capture a single chemical species (chemistry fit) in the complex spectra. Herein, this approach is compared to an envelope fit approach using Biesinger multiplet components of known iron oxides to determine how effective these methods are in reproducing iron oxide composition. Mixed oxide and metal XPS Fe 2p spectra were synthesized using reference spectra collected experimentally. For the first time, the accuracy and differences between the two approaches are reported. It is demonstrated that no meaningful conclusions can be drawn using single symmetric peaks to analyze complex Fe 2p3/2 spectra, implying that a large portion of the literature is flawed. The envelope fit approach, however, is shown to provide useful information regarding oxide ratios in mixed iron oxide materials, though limitations do exist. A methodology for evaluating the quality of XPS analysis of Fe 2p3/2 spectra is proposed for benchmarking new submissions so that reviewers, authors, and editors can assess these submissions. [ABSTRACT FROM AUTHOR]

The present study focuses on the elaboration of magnetic nanocomposites by the in situ incorporation of magnetite (Fe3O4) nanoparticles (NPs) with spherical and nanoflower-like morphologies in graphitic carbon nitride (g-C3N4) sheets using two different synthetic routes. Nanomaterials are characterized by TEM, SEM, XRD, FTIR, BET, zetametry, vibrating sample magnetometry, and UV–vis absorption spectroscopy. The decoration of the carbon nitride matrix with the magnetic NPs enhanced optical and textural properties. The influence of the morphology of the magnetic NPs on the adsorptive and photocatalytic properties of the nanocomposites under different pH conditions (4.5, 6.9, and 10.6) was assessed from batch tests to remove methylene blue (MB) from aqueous solutions. In extreme pH conditions, the nanocomposites exhibited lower or equivalent MB removal capacity compared to the pure g-C3N4. However, at neutral medium, the nanocomposite with incorporated Fe3O4 nanoflowers showed a significantly higher removal efficiency (80.7%) due to the combination of a high adsorption capacity and a good photocatalytic activity in this pH region. The proposed nanocomposite is a promising alternative to remove cationic dyes from water by magnetic assistance, since no pH adjustment of the polluted effluent is required, reducing costs and environmental impact in the dyeing industry. [ABSTRACT FROM AUTHOR]

This study successfully synthesized Fe2O3@rGO nanocrystals using a straightforward sol-gel method in a pigskin-gel (gelatin type A) environment. The fabricated nanocomposites include Fe2O3-linked nanosheets in a reduced graphene oxide-like double tetrahedral pyramid (DTP) structure and Fe2O3 nanocrystals resembling Cheetos puffs (CPs). The Fe2O3@rGO material was characterized through a variety of analytical techniques, including X-ray diffraction, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, elemental mapping, Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, Raman spectroscopy, vibrating sample magnetometer, nitrogen physisorption, and electrochemical impedance spectroscopy. The photocatalytic efficiency of Fe2O3 and Fe2O3@rGO samples in demineralizing rhodamine B in an aqueous solution was thoroughly evaluated. Remarkably, the Fe2O3@rGO composites exhibited significantly enhanced photocatalytic activity and degradation efficiency compared to pure Fe2O3 nanocrystals. The improved performance can be attributed to effective electron transport between the reduced graphene oxide and the semiconductors, effectively reducing electron-hole recombination. Additionally, the Fe2O3@rGO nanocrystals demonstrated excellent magnetic properties, enabling easy separation and recovery after five cycles of reusability testing. These findings highlight the promising potential of this magnetic nano photocatalyst for efficient and sustainable wastewater treatment applications, particularly in the degradation of rhodamine B. Highlights: In the presence of pigskin gel, the synthesis of Fe2O3 nanocrystals (NCs) resembling Cheetos puffs (CPs) were carried out. In the presence of pigskin gel as a reducing agent, Fe2O3 nanocrystals with double tetrahedral pyramidal geometry (DTP) attached to reduced graphene oxide (rGO) nanosheets were obtained. Fe2O3@rGO:DTP Showed improved responsiveness compared to the pure Fe2O3:CPs for the degradation of organic pollutants. [ABSTRACT FROM AUTHOR]

Cancer is a global issue and hence various efforts are being made. Iron oxide is considered a significant biochemical agent in the biomedical arena for cancer treatment. Marine macroalgae-mediated iron oxides especially, magnetite (Fe3O4) nanoparticles (NPs) are a prospective alternative to diagnose and treat cancer owing to their fluorescent and magnetic properties. We intend to appraise the usability of the aqueous extract of Rosenvingea intricata (R. intricata) in Fe3O4 NPs synthesis and to study their cytotoxic effects against human hepatocarcinoma (Hep3B) and pancreatic (PANC1) cancer cells. In the present study, R. intricata were collected from the coastal region of South Andaman, India. Aqueous extracts of R. intricata were utilized to synthesize Fe3O4 NPs via the co-precipitation method. Phycosynthesized Fe3O4 NPs exhibited wide peak at 400–600 nm from ultraviolet–visible diffused reflectance spectroscopic analysis which validated the formation of NPs. Band edge emission peak at 660 nm in fluorescent spectra confirmed the quantum confinement in Fe3O4 NPs. Fourier transform infrared spectroscopy confirmed the role of R. intricata as a capping and reducing agent with functional groups such as O–H, C–H, C=O, N=O, C=C, C–O, C–N, and C–S arising from amino acids, polysaccharides, aliphatic hydrocarbons, esters, amides, lignins, alkanes, aliphatic amines, and sulfates. Physicochemical properties such as crystallite size (14.36 nm), hydrodynamic size (84.6 nm), irregular morphology, elemental composition, particle size (125 nm), crystallinity, and saturation magnetization (0.90007 emu/g) were obtained from x-ray diffractometer, dynamic light scattering, scanning electron microscopy, energy dispersive x-ray spectrometer, high-resolution transmission electron microscopy, selected area electron diffraction and vibrating sample magnetometer techniques, respectively. The cell viability showed dose-dependent cytotoxic effects and enhanced the apoptosis against Hep3B and PANC1 cancer cells. R. intricata extract capped Fe3O4 NPs could be the most appropriate and effective nanomaterial for cancer treatment and management. [ABSTRACT FROM AUTHOR]

Perovskite oxides play a crucial role as catalysts in the oxygen evolution reaction (OER) owing to their distinctive structure and diverse physical and chemical characteristics. Currently, enhancing the electronic structure and specific surface area of the perovskite surface through strategic regulation poses a significant challenge in the advancement of perovskite catalyst development. Here, we propose a novel method for enhancing the OER activity of LaCoO 3 (LCO) perovskite through atomic doping and interface engineering. The La 0.6 Sr 0.4 CoO 3 –FeOOH (Fe-LSCO) composite exhibits a notable enhancement in electrocatalytic performance, manifesting a low overpotential of 296.3 mV for the oxygen evolution reaction (OER) at a current density of 10 mA cm−2, while maintaining a high level of activity for a duration of 120 h. The enhanced activity of Fe-LSCO can be attributed to oxygen vacancy defects and the increase of the active site caused by A-site-doping and amorphous nanosheets of FeOOH, which synergistic effect reduces the energy barrier for water dissociation. The highly disordered surface and high surface energy of amorphous FeOOH render it highly active. This study presents a viable interface engineering approach for manipulating the reconstruction of the active phase in high-performance perovskite-based electrocatalytic materials. [Display omitted] • Sol-gel and solution soaking treatment were used to fabricate Fe-LSCO. • The doping of Sr changes the spin state of Co ion. • The amorphous hydroxyl iron oxide can improve hydrophilicity and BET. • Fe-LSCO electrode demonstrates outstanding durability and stability. [ABSTRACT FROM AUTHOR]

Iron silver oxide (AgxFe2−xO3; 0xFe2−xO3 shown in the figure can be indexed to the hexagonal structure of silver oxide and the rhombohedral structure of hematite and new X-ray Diffraction (XRD) peaks of AgxFe2−xO3 structure. The annealing and doping process seems to cause a serious change in the crystal structure of the thin film, it showed a serious change in its electrical properties. The electrical parameters of resistance for thin films were measured using the Hall measurement method at room temperature. With Hall measurements, the n-type carrier concentration of the Fe2O3 structure was calculated, and it was observed that its resistance was 1MΩ. Likewise, it was observed that AgxFe2−xO3 exhibited an n-type carrier concentration, and its resistance was calculated to be 0.5MΩ. The conductivity change is based on silver doping. The doping process seems to cause a change in the bandgap of the thin film, it showed a change in its optical properties. The film’s optical absorption was measured by UV–Vis photo spectroscopy. Subsequently, the structural and topographic properties of AgxFe2−xO3 structures were investigated by high-precision characterization devices. [ABSTRACT FROM AUTHOR]

This study focuses on developing machine learning models to detect subtle alterations in hepatocyte chromatin organization due to Iron (II, III) oxide nanoparticle exposure, hypothesizing that exposure will significantly alter chromatin texture. A total of 2000 hepatocyte nuclear regions of interest (ROIs) from mouse liver tissue were analyzed, and for each ROI, 5 different parameters were calculated: Long Run Emphasis, Short Run Emphasis, Run Length Nonuniformity, and 2 wavelet coefficient energies obtained after the discrete wavelet transform. These parameters served as input for supervised machine learning models, specifically random forest and gradient boosting classifiers. The models demonstrated relatively robust performance in distinguishing hepatocyte chromatin structures belonging to the group exposed to IONPs from the controls. The study's findings suggest that iron oxide nanoparticles induce substantial changes in hepatocyte chromatin distribution and underscore the potential of AI techniques in advancing hepatocyte evaluation in physiological and pathological conditions. [ABSTRACT FROM AUTHOR]

AbstractThe major aim of this research hyperthermia and magnetic resonance-high intensity focused ultrasound (MR-HIFU) focused on investigating the potential of aloe vera leaf extract-mediated gold-coated iron oxide nanohybrids (Au-IONPs) as a modern theragnostic material for the treatment of uterine myoma. To assess the cytotoxicity of Au-IONPs, induce hyperthermia, and apply radiotherapy to determine the level of apoptosis in the human ht-UtLM cells. Subsequently, it evaluated the cytotoxicity of the nanoparticles on human ht-UtLM cells by exposing the cells to various concentrations of Au-IONPs for a 4-hour incubation period. Based on the results, concentrations of 10 and 15 µg/mL were selected for further investigation. The MTT assay and flow cytometry results demonstrated that Au-IONPs significantly induce cell apoptosis. It allows the Au-IONPs to turn as an effective development mediator in the ablation of high-intensity focused ultrasound (HIFU) treatment. Finally, it could be suggested to developed material have excellent systemic toxicity, which promises well for treatment of uterine fibroids.HIGHLIGHTSBiosynthesis of gold – iron oxide nanohybrids (Au-IONPs) through a green approach.Physio-chemical properties of Au-IONPs have been characterized through various techniques.Investigating the anti-tumor effects of Au-IONPs in combination with thermo-radiotherapy for uterine myoma.Determine the level of apoptosis in the human myoma cells by inducing hyperthermia and radiotherapy.Observed the correlation behavior between the dose of the cell viability and Au-IONP nanoparticles.Au-IONPs had a significant impact on enhancing the effects of both hyperthermia and radiation therapies.Biosynthesis of gold – iron oxide nanohybrids (Au-IONPs) through a green approach.Physio-chemical properties of Au-IONPs have been characterized through various techniques.Investigating the anti-tumor effects of Au-IONPs in combination with thermo-radiotherapy for uterine myoma.Determine the level of apoptosis in the human myoma cells by inducing hyperthermia and radiotherapy.Observed the correlation behavior between the dose of the cell viability and Au-IONP nanoparticles.Au-IONPs had a significant impact on enhancing the effects of both hyperthermia and radiation therapies. [ABSTRACT FROM AUTHOR]

Underground hydrogen storage (UHS) has been considered as an integral part of energy transition from fossil fuels to renewable sources. Porous aquifers can serve as typical sites for this purpose due to their worldwide distribution and huge storage capacity. However, the diverse microbial species that inhabit the aquifers are known to be able to catalyze in-situ biochemical reactions within the hosting rock. These reactions can normally lead to microbial consumption of hydrogen, microbial clogging of pore space and thus affect hydrogen injection and withdrawal rates as reported in the literature. So far, these phenomena have been widely reported but rarely quantified. In this study, we build a coupled hydrological-mechanical-chemical-biological (HMCB) multiphysics model to simulate these microbe-related processes during UHS in aquifers. The model consists of a complete set of partial differential equations to describe: (1) rock deformation; (2) water-hydrogen two-phase flow; (3) microbes and dissolved hydrogen transport; (4) mineral dissolution/precipitation; and (5) microbial activities involving adsorption/desorption and growth/decay. All these processes are linked together through the porosity/permeability models which consider the joint impacts of microbial clogging, mineral dissolution/precipitation and effective stress. This multiphysics model is verified against laboratory biochemical reaction data and microbial transport data. Then, the verified model is used to investigate the impacts of iron-reduction bacteria (IRB) activities on UHS in aquifers. Based on the simulation results, it can be concluded that (1) hydrogen saturation at the top surface of the aquifer is the greatest while microbial activities surrounding the injection well is stimulated the most; (2) microbial activities influence the initial few cycles of hydrogen injection and withdrawal but the impacts gradually diminish with the dissolution of Fe 2 O 3 ; (3) hydrogen recovery efficiency is degraded due to the combined effects of hydrogen consumption, water production and microbial clogging with the microbial clogging impact being the most significant; and (4) effective stress impacts aquifer permeability throughout UHS operations while microbial clogging influences it in the initial few cycles. For mineral dissolution/precipitation, the impact can be neglected. • Coupled multiphysics model has been developed to quantify the impact of IRB activities on UHS in aquifers. • Interactions among hydraulic-mechanical-chemical-biological processes are captured. • The model has been verified against laboratory microbial transport data and chemical reaction data. • Dependence of hydrogen recovery performance on various microbe-related parameters are evaluated. [ABSTRACT FROM AUTHOR]

α-Fe 2 O 3 has been regarded as an ideal n-type photoanode material due to its exceptional stability, environmental friendliness, optimal band structure (1.9∼2.2 eV), and valence band position (approximately 2.3 V). However, α-Fe 2 O 3 still faces challenges such as low absorption coefficient, poor conductivity, short carrier lifetime, low carrier mobility, facile recombination of photogenerated charges, and sluggish kinetics of water oxidation. To address these issues comprehensively and effectively, this study initially synthesized Ti-doped Fe 2 O 3 nanorods through doping and hydrothermal methods. Subsequently, a PdCoP amorphous layer was deliberately fabricated on the Ti:Fe 2 O 3 nanorods (TF) photoelectrode through facile solution impregnation and phosphorization treatment. The experimental results demonstrate that Ti doping effectively enhances carrier separation, leading to a photocurrent of 0.52 mA cm−2 at 1.23 V RHE , which is 2.08 times higher than the undoped counterpart. Moreover, upon further modification with the PdCoP amorphous layer, the photocurrent density of PdCoP/TF photoanode significantly increases under illumination, reaching 2.82 mA cm−2 at 1.23 V RHE , which is 11.28 times higher than pure Fe 2 O 3. Density functional theory (DFT) calculations performed at the interface between the amorphous layer and substrate indicate that surface modification of PdCoP on TF alters its surface electronic structure while reducing the energy barrier for oxygen evolution reaction (OER), thereby enhancing its performance in photoelectrochemical water splitting. [Display omitted] • The electronic structure of α-Fe 2 O 3 is optimized through Ti doping and modification of the amorphous layer. • The PdCoP/TF photoanode exhibits high efficiency in converting solar energy. • Revealing the active sites and mechanisms for water splitting through DFT calculations. [ABSTRACT FROM AUTHOR]

Although spinel ferrite nanostructures with adjustable magnetic properties have long been considered for different applications such as microwave, biomedical and magnetic memory devices, detailed magnetic behavior and structural properties of manganese-cobalt ferrites are yet to be investigated and understood. Here, cobalt ferrite nanoparticles (NPs) substituted with manganese (Co1–x Mnx Fe2O4); 0 ≤ x ≤ 1) are synthesized using a co-precipitation method followed by annealing at 800 °C. X-ray diffraction patterns confirm the formation of cubic spinel structure, which is accompanied with α-‌ Fe 2 O 3 secondary phase when increasing the manganese content of NPs, as also observed using field emission scanning electron microscopy. Hysteresis loop measurements demonstrate an increasing trend of magnetic properties with increasing x, leading to maximum values of saturation magnetization (Ms= 65 emu/g) and coercivity (Hc= 1815 Oe) for Co 0.8 Mn 0.2 Fe 2 O 4 NPs. Meanwhile, first-order reversal curve (FORC) analysis manifests distinct soft and hard magnetic phases induced by the slight enhancement in the manganese content. The magnetic hardening of single domain manganese-cobalt ferrite NPs at room temperature is revealed by an increase in FORC coercivity up to 2480 Oe, being about 90% higher than that for pure cobalt ferrite NPs. Further increasing x weakens magnetic properties, minimizing M s and H c to 10 emu/g and 35 Oe when Mn completely substitutes Co in the spinel ferrite structure. In this case, FORC analysis shows suppressed inter-particle magnetostatic interactions and predominant superparamagnetic contribution for MnFe 2 O 4 NPs. [ABSTRACT FROM AUTHOR]

This study focused on developing self-cleaning matte ceramics based on polycrystalline hexaferrite for oil removal. The ceramics were glazed using glaze materials BaO, Fe 2 O 3 , ZnO, and TiO 2 with varying ZnO:TiO 2 ratios. The aim of this research was to determine the glaze composition that was able to provide the best self-cleaning/PA removal characteristics. After calcination at 1200°C, a polycrystalline hexaferrite compound formed, BaFe 12 ZnTiO 19. All ceramic samples demonstrated palmitic acid (PA) photodegradation, with CM3 (ZnO:TiO 2 ; 1:1) showing the highest efficiency. This efficiency correlated with CM3's lowest bandgap of 1.43 eV. The photodegradation of PA by CM3 follows first-order kinetics with rate constants of 0.0482 min−1 under UV irradiation and 0.0179 min−1 under visible irradiation. CM3 displayed exceptional durability, maintaining PA removal even after prolonged use, making it optimal for practical applications. [ABSTRACT FROM AUTHOR]

The electrocatalytic recycling of waste nitrate (NO3RR) is a promising decentralized route for green ammonia synthesis. Nonetheless, it suffers from the competing hydrogen evolution reaction and the insufficient proton supply in high pH conditions. Herein, iron oxide nanoparticles anchored on ZnO is introduced as a strategy to enhance the water dissociation ability and proton transfer rate, advancing NH4+ production from alkaline NO3RR. Supported by a set of ex situ and in situ characterization, the findings reveal the reduction of iron oxides, along with improvements in charge transfer properties and proton generation from H2O. Theoretical calculations show that iron oxides reduce the kinetic barrier of the rate‐limiting step (*NO2‐to‐*NO2H) and result in a thermodynamically favorable process to hydrogenation steps, which in turn reduce the overall energy barrier of alkaline NO3RR. Optimal catalytic activity is realized with a Fe loading of 0.5 wt.%, delivering a Faradaic efficiency of ≈83% for ammonium with a NH4+ yield rate of 31 nmol s−1 cm−2 at −0.7 V versus RHE. The results pave the way for the utilization of bi‐metal interaction to tune the reaction pathway for achieving sustainable ammonium synthesis in alkaline, contributing to ongoing efforts to achieve a sustainable nitrogen cycle via N‐based electrochemistry. [ABSTRACT FROM AUTHOR]

Previously, a strategy for doping MIEC perovskites ABO 3-δ with highly charged cations B5+ (Nb, Ta) and B6+ (Mo, W) was developed. The doping strategy is based on the idea that strontium ferrite/cobaltite-based perovskites are ferroelastic, whereas highly charged cations are ferroactive species. An increase in the concentration of the dopant leads to a reduction in the size of the domains of the ferroelastic phase down to the nanoscale. This resulted in the smearing of phase transitions with the formation of the highly conductive glassy state. Tantalum-doped lanthanum-strontium-ferrite perovskite (La 0.6 Sr 0.4 Fe 1-x Ta x O 3-δ , LSFTx) was prepared via solid-state reaction using chemically pure oxide powders of La 2 O 3 , SrCO 3 , Fe 2 O 3 , and Ta 2 O 5 , followed by calcination and sintering up to 1350 °C. The structural and surface properties were examined using X-ray diffraction and a scanning electron microscope. The original oxygen partial pressure relaxation (OPPR) method was used to study the kinetic properties of LSFTx. Continuous equilibrium phase diagram "T – pO 2 – δ" first obtained by oxygen release technique for composition LSFT3.5. Power law dependencies of the kinetic properties on the oxygen partial pressure are presented. [ABSTRACT FROM AUTHOR]

Copper-promoted iron oxides are commonly utilized in high-temperature water-gas shift (WGS) reactions. Although the promotional effect of Cu has been previously documented, the nature of the active sites for Cu/Fe 3 O 4 remains debated and the role of the crystallite size of Fe 3 O 4 has not been tackled. In this study, a wide range of Cu/Fe 3 O 4 catalysts were designed by hosting Cu species onto Fe 3 O 4 of two contrasting crystallite sizes (approximately 10 and 160 nm) and by utilizing different preparation methods (ammonia evaporation and deposition-precipitation). The evaluation of their catalytic WGS performances revealed a remarkable and previously undocumented phenomenon: the addition of Cu resulted in universal activity enhancements only for small Fe 3 O 4 crystals, while the larger analogues displayed decreased activity. This peculiar phenomenon can be explained by the creation of Cu–Fe 3 O 4 interfaces present in the iron oxides of small crystallite sizes. Thorough characterizations, such as advanced electron microscopic, in situ powder X-ray diffractions, in situ diffuse reflectance infrared Fourier transform spectroscopy, and computational studies, suggest strong electronic interactions between the different metal species, facilitated reductions of the individual oxides, and more favorable CO activation at the interfacial sites, all accounting for the promoted activity. [Display omitted] • Influence of Fe 3 O 4 crystallite size in water-gas shift reaction was examined. • Performance of Cu/Fe 3 O 4 in water-gas shift reaction was studied. • The formation of Cu–Fe 3 O 4 interfaces existed on small Fe 3 O 4 crystals. • Promotional effect of Cu was only found on small Fe 3 O 4 crystals. [ABSTRACT FROM AUTHOR]

The study of the cementitious material activity of industrial solid wastes is a key issue in the comprehensive utilization of its green building materials. In this study, mechanical activation was used to prepare cementitious materials from vanadium-titanium iron ore tailings (VTIOT) as the main raw materials, and the effects of grinding time, the key parameter, on the grinding characteristics of VTIOT, the mechanical properties of the VTIOT cementitious material, and the hydration mechanism were investigated by means of surface area analysis, particle size analysis, X-ray diffraction (XRD), scanning electron microscopy (SEM), alkali leaching, mechanical testing, hydration heat analysis, and thermogravimetric analysis (TGA). The results show that: the grinding time and specific surface area of VTIOT exhibit a linear correlation. Prolonging the grinding time, the fractal dimension of the particles gradually increases. The activity of Si4+ and Al3+ elements increases rapidly, reaching a Si4+ and Al3+ content of 96 mg·L−1 at 90 min of grinding. With a VTIOT mixing amount of 30 %, a mortar paste ratio of 1:3, and a water cement ratio of 0.5, the 50 min ground VTIOT mortar demonstrates 7 d and 28 d compressive strengths of 29 MPa and 38.7 MPa, corresponding to the highest values of the activity index, measured at 71.4 % and 75.2 %, respectively. Under standard curing conditions, the hydration products of cementitious materials at 7 d are ettringite (AFt), calcium silicate hydrate (C-S-H), alumina, ferric oxide, monsulfate (AFm), calcium hydroxide (Ca(OH) 2), and calcium silica (CS). In the hydration process of 7 d, the exothermic peak and exothermic amount of the 50 min VTIOT cementitious materials are greater than those observed for other grinding times, but lower than those of pure reference cement. [ABSTRACT FROM AUTHOR]

The Cr(VI) removal efficiency of a Brazilian Oxisol collected from the A horizon (15.2% iron oxides, 4.6% organic matter, pH 4.3) was assessed and compared with synthesized iron minerals (SM), to mitigate contamination as a nature-based solution. Batch tests revealed that Cr(VI) removal efficiency was higher and faster for SM than for Oxisol: to remove ∼ 100% Cr(VI) from a solution containing 5 mg L− 1Cr(VI), SM took 24 h, while for the same concentration Oxisol removed 80% Cr(VI) in 30 days. At a higher concentration (30 mg L− 1), Cr(VI) removal efficiency dropped to 90% in 24 h for SM and 22% in 30 days for Oxisol. The Cr(VI) removal of Oxisol and SM fitted, respectively, to the pseudo-first and pseudo-second order, reflecting the way Cr(VI) is removed - by adsorption for SM (since pHPZC> pHsolution) and by reduction to Cr(III) for Oxisol organic matter. To simulate a contamination event, Oxisol was incubated with 300 mg L− 1 of Cr(VI) for 5, 10 and 30 days, followed by sequential extraction. The results of this test revealed that all the chromium was reduced to Cr(III) in all the time periods, and was mostly bound to the less mobile fractions of the soil: organic matter (75–85%), iron oxide/hydroxide (∼ 15%), and the residual fraction (< 5%); and only 5–10% was bound to the exchangeable fraction (more mobile). Although Cr(VI) is better adsorbed by SM, in Oxisol chromium is found in the less toxic form (trivalent) and bound to the less mobile fractions, promoting a more sustainable solution. [ABSTRACT FROM AUTHOR]

Fluorinated arylborane‐based Lewis acid catalysts have shown remarkable activity and serve as ideal examples of transition metal‐free catalysts for diverse organic transformations. However, their homogeneous nature poses challenges in terms of recyclability and separation from reaction mixtures. This work presents an efficient technique for the heterogenization of boron Lewis acid catalysts by anchoring Piers' borane to allyl‐functionalized iron oxide. This catalyst demonstrates excellent activity in the hydrosilylation of imines and the reductive amination of carbonyls using various silanes as reducing agents under mild reaction conditions. The catalyst exhibits broad tolerance towards a wide range of functional substrates. Furthermore, it exhibits good recyclability and can be easily separated from the products using an external magnetic field. This work represents a significant advance in the development of sustainable heterogenous metal‐free catalysts for organic transformations. [ABSTRACT FROM AUTHOR]