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The adsorption and dissociation of CO2 on both perfect and oxygen-deficient α-Cr2O3 (0001) surfaces, alongside the subsequent incorporation of the resulting C into the oxide lattice and its impact on oxide growth, are investigated using first-principles calculations. Our findings reveal that oxygen vacancies significantly enhance CO2 adsorption and promote its stepwise decomposition into C and O atoms. The resulting C can spontaneously dissolve into the oxide lattice through the oxygen vacancies. The presence of bulk dissolved C in the Cr2O3 lattice substantially enhances the formation, migration, and clustering of oxygen vacancies in the bulk. These results provide an atomic-level understanding of how CO2 accelerates the oxidation of chromia-forming alloys, offering microscopic insights for controlling oxide growth and mitigating oxidation-induced degradation of high-temperature alloys. [ABSTRACT FROM AUTHOR]

Some spinel chromium oxides with the chemical formula ACr2O4 exhibit magnetic-induced multiferroicity due to the special spiral spin order. However, because of the relatively low temperature of the ordered spiral phase, this kind of multiferroicity generally displays a limited coexistence of magnetic and ferroelectric orders in a narrow temperature range. The Jahn–Teller (JT) effect, serving as a crucial link between charge and orbit degrees of freedom, can facilitate efficient modulation of multiferroic properties. In this work, Ni1−xCuxCr2O4 (0 ≤ x ≤ 0.2) series are synthesized by occupying the same Wyckoff site with two kinds of JT ions. The microstructure and JT distortion can be distinctly influenced by varying the doping level of Cu2+ ions. Particularly, Ni0.85Cu0.15Cr2O4 (x = 0.15) presents the pronounced JT distortion, accompanied by observation of dielectric anomaly at ∼78 K, resulting from spin–orbit coupling. This implies that the JT effect can significantly promote the contribution of spin–orbit coupling in magnetoelectric correlation. Moreover, the magnetodielectric effect induced by intrinsic magnetoelectric coupling is confirmed in Ni0.85Cu0.15Cr2O4 over a wide temperature range of 10–200 K, which is much higher than the Néel temperature of ∼85 K. It indicates that spin–orbit coupling based on the JT effect could overcome the constraint of magnetic order to achieve effective control on electric polarization performance under an applied magnetic field, thereby showing broad application prospects. [ABSTRACT FROM AUTHOR]

This work outlines conditions suitable for the heteroepitaxial growth of Cr2O3(0001) films (1.5–20 nm thick) on a Ru(0001)-terminated substrate. Optimized growth is achieved by sputter deposition of Cr within a 4 mTorr Ar/O2 20% ambient at Ru temperatures ranging from 450 to 600 °C. The Cr2O3 film adopts a 30° rotated honeycomb configuration with respect to the underlying Ru(0001) substrate and exhibits a hexagonal lattice parameter consistent with that for bulk Cr2O3(0001). Heating to 700 °C within the same environment during film preparation leads to Ru oxidation. Exposure to temperatures at or above 400 °C in a vacuum, Ar, or Ar/H2 3% leads to chromia film degradation characterized by increased Ru 3d XPS intensity coupled with concomitant Cr 2p and O 1s peak attenuations when compared to data collected from unannealed films. An ill-defined but hexagonally well-ordered RuxCryOz surface structure is noted after heating the film in this manner. Heating within a wet Ar/H2 3% environment preserves the Cr2O3(0001)/Ru(0001) heterolayer structure to temperatures of at least 950 °C. Heating an Ru–Cr2O3–Ru heterostacked film to 950 °C within this environment is shown by cross-sectional scanning/transmission electron microscopy (S/TEM) to provide clear evidence of retained epitaxial bicrystalline oxide interlayer structure, interlayer immiscibility, and epitaxial registry between the top and bottom Ru layers. Subtle effects marked by O enrichment and O 1s and Cr 2p shifts to increased binding energies are noted by XPS in the near-Ru regions of Cr2O3(0001)/Ru(0001) and Ru(0001)/Cr2O3(0001)/Ru(0001) films after annealing to different temperatures in different sets of environmental conditions. [ABSTRACT FROM AUTHOR]

This study presents the comparison of microstructure, mechanical, tribological, and optical properties of the ternary chromium-aluminum oxide films ((Cr 1-x Al x) 2 O 3) with binary Cr 2 O 3 and Al 2 O 3 films, deposited by atomic layer deposition at 275 °C. The atomic growth per cycle of the Al atoms increased from 3.1 to 8.5 atoms/nm2 on chromium oxide film. The Al 2 O 3 films were X-ray amorphous. The Cr 2 O 3 films contained crystallites of the eskolaite phase. Nano-size (diameter from 3 to 5 nm) crystallites with cubic symmetry and matching with that of cubic γ-Al 2 O 3 or η-Al 2 O 3 phases were observed in (Cr 1-x Al x) 2 O 3 films. The ternary film with Al/(Al + Cr) of 0.40 showed the highest hardness (18.4 GPa) and elastic modulus (169.4 GPa), whereas the wear rate of this film decreased by ∼80 % compared with Cr 2 O 3 films. Optical band gap energy values corresponding to the indirect transition model decreased from 2.93 eV for the Cr 2 O 3 film to 2.58 eV for the Cr-Al-O films. [Display omitted] • The process of atomic layer deposition of (Cr 1-x Al x) 2 O 3 films was studied. • Nanocrystallites with size of 3–5 were observed in (Cr 1-x Al x) 2 O 3 films. • The increase in hardness and elastic modulus for (Cr 1-x Al x) 2 O 3 films was observed. • The wear resistance of the ternary films improved by about 80 % compared with Cr 2 O 3. • Changes in optical properties of the Cr 2 O 3 films were detected by doping with Al. [ABSTRACT FROM AUTHOR]

The microstructural evolution of T91 steel by pre-steam oxidation during liquid lead-bismuth eutectic (LBE) dissolution corrosion was investigated. A bi-layered pre-oxide film with Fe-rich outer layer and Cr-rich inner layer was formed on T91 steel, which was similar to the oxide film of T91 after oxidation corrosion in LBE. The pre-oxide film effectively protects the matrix from LBE corrosion at 620 °C. However, the composition and microstructure of the pre-oxide film changed dramatically. Unlike the original duplex structure, the pre-oxide film exposed to LBE undergoes a process of reduction of the outer layer and oxidative growth of the inner layer and changes into five layers, the loose and easily peeling outer Fe layer, the dense and intact inner layers successively consisting of Fe–Cr spinel layer, a transition layer of matrix and Cr-rich oxide, continuous Cr-rich oxide layer with tetragonal distorted spinel structure and amorphous SiO2 layer. The evolution mechanism of the pre-oxide film during LBE dissolution corrosion is discussed. [ABSTRACT FROM AUTHOR]

Model alloy, Fe-20Cr (wt%), was oxidized in two gas mixtures Ar-5H2O-(5H2) (vol%) at 850 °C. The alloy formed Cr2O3 scales in both gases. The Cr2O3 scale developed faster in Ar-5H2O-5H2 and contained fine pores, whilst that grown in Ar-5H2O was dense. Experiments with inert SiO2 marker revealed that the Cr2O3 scale growth in Ar-5H2O-(5H2) was controlled mainly by outward Cr diffusion. When adjusted for grain boundary diffusion effects, Wagner's theory was successful in describing the hydrogen effect, provided that the Cr2O3 scales are n-type. [ABSTRACT FROM AUTHOR]

This study investigates the delubrication, reduction, and decarburization processes of powder metallurgical steel alloys (CrM, CrL, AHC, Mo85, SintD 35) and an unalloyed steel during sintering in a pure hydrogen atmosphere. Utilizing in-situ FTIR gas phase analysis, components with ethylenebisstearamide (EBS) as a lubricant are analyzed. EBS decomposition in steel components yields CO, CO2, H2O, and CH4, with dominant CH groups observed in the 230 °C to 480 °C range. In the temperature range between 750 °C and 850 °C, where CO formation is expected due to the reduction of surface iron oxides, CH4 is present instead, indicating that an "internal getter effect" also occurs in pre-alloyed powders. In addition, with high carbon activity, the reduction of internal iron oxides and the reduction of chromium oxides also trigger an internal getter effect. Depending on the carbon potential, these processes cause a considerable reduction in the carbon content of the powder metallurgical components. The study therefore shows that the decarburization of powder metallurgical components during the heat treatment phases prior to sintering in a 100 pct hydrogen atmosphere is less due to the mechanism of delubrication, but rather to mechanisms of carbothermal reduction. [ABSTRACT FROM AUTHOR]

Prereduction process of chromite is an effective method for saving energy and reducing emissions during ferrochrome alloy production. This study investigates the factors affecting the reduction and strength levels of chromite pellets reduced in a CH4–H2 atmosphere. Thermodynamic calculations indicate that carbon from methane pyrolysis is highly active, and chromium oxide can be converted to metal chromium and carbide at lower temperature of 1100 °C. The experimental results show that extending the reduction time can increase the pellet metallization rate without sacrificing strength at 1100 °C in 10% CH4. As the reaction progressed, the carbon from methane cracking diffused into the pellet through the metallic iron, creating observable diffusion channels. Continuous methane input further facilitates this mechanism, leading to iron carbide precipitation and ultimately compromising the pellet strength. The consolidation mechanism of pellets in CH4–H2 = 10:90 atmosphere is analyzed using X‐ray diffraction, scanning electron microscopy‐energy dispersive X‐ray spectroscopy, and chemical analysis. The consolidation process of the pellets can be divided into four stages—namely, liquid phase formation, phase transition, strengthening, and carbonization stages. [ABSTRACT FROM AUTHOR]

AbstractThe present study rigorously examined the toxicological effects of nanoparticles (NPs), specifically nickel (Ni) and chromium oxide (Cr3O4) NPs, synthesized under controlled conditions and characterized. To evaluate their potential environmental impact exposed the freshwater fish Labeo rohita (L. rohita) to environmentally relevant concentrations of both NPs within a controlled laboratory conditions. Vital organs, including gills and liver were subjected to histopathological analysis, revealing profound alterations in tissue architecture that were distinctly correlated with pathological damage. The lesions exhibited moderate to severe changes that are further correlated with the semi-quantitative mean alteration value (MAV). Furthermore, conducted a quantitative assessment of tissue-specific morphological changes. Notably, there was a significant reduction in critical hematological changes, including red blood cell (RBC) and white blood cell (WBC) counts, hemoglobin concentrations and other parameters. All of which exhibited significant fluctuations in relation to increasing NPs concentrations. These findings underscore the critical necessity for continued investigation into the ecological risks associated with these nanoparticles. [ABSTRACT FROM AUTHOR]

Chromia (Cr2O3) is a magnetoelectric oxide that permits voltage‐control of the antiferromagnetic (AFM) order, but it suffers technological constraints due to its low Néel Temperature (TN ≈307 K) and the need of a symmetry‐breaking applied magnetic field to achieve reversal of the Néel vector. Recently, boron (B) doping of Cr2O3 films led to an increase TN >400 K and allowed the realization of voltage magnetic‐field free controlled Néel vector rotation. Here, the impact of B doping is directly imaged on the formation of AFM domains in Cr2O3 thin films and elucidates the mechanism of voltage‐controlled manipulation of the spin structure using nitrogen‐vacancy (NV) scanning probe magnetometry. A stark reduction and thickness dependence of domain size in B‐doped Cr2O3 (B:Cr2O3) films is found, explained by the increased germ density, likely associated with the B doping. By reconstructing the surface magnetization from the NV stray‐field maps, a qualitative distinction between the undoped and B‐doped Cr2O3 films is found, manifested by the histogram distribution of the AFM ordering, that is, 180° domains for pure films, and 90° domains for B:Cr2O3 films. Additionally, NV imaging of voltage‐controlled B‐doped Cr2O3 devices corroborates the 90° rotation of the AFM domains observed in magnetotransport measurement. [ABSTRACT FROM AUTHOR]

Field exposure for 5000h combined with weight gain measurement and morphology/composition analysis of oxide film were conducted to examine high temperature oxidation behavior of GH4169 and In617 nickel-based super alloys in SOFC system environment. The In617 alloy has been found to demonstrate excellent oxidation resistance in the SOFC environment because of its high Ni content. An integral and dense NiO oxide film can be developed in the outer layer with a continuous Cr 2 O 3 oxide film formed in inner layer. It indicates that NiO played a crucial role in the formation of an integral and dense oxide film. In contrast, GH4169 alloy failed to develop a continuous and dense oxide film probably due to high Fe content, in which case Fe-dopped chromium oxide (Fe,Cr) 2 O 3 was formed. As a result, the oxide film was loose and porous, leading to relatively poor oxidation resistance. • NiO played a crucial role in the formation of an integral and dense oxide film. • Fe is harmfull for oxidation resistance of nickel-based alloy. • The dopping of Fe in Cr 2 O 3 could result in loose and porous structure of the chromia. [ABSTRACT FROM AUTHOR]

The current method for recovering iron oxide scale in the steel industry is not economically optimal, especially for high‐alloy scales found in alloyed steel. This study focuses on iron oxide scale containing valuable metals like chromium (Cr), molybdenum (Mo), and vanadium (V). The required carbon addition is calculated based on the iron and chromium oxides in the scale. The effects of varying carbon additions and reduction temperatures on reduction efficiency are thoroughly examined. Kinetic studies show that as temperature and carbon increase, the rate‐limiting step shifts from interfacial diffusion to interfacial reaction. Reduction experiments assess carbon utilization, metallization rate, deoxidation rate, and removal of harmful elements. Results show that high temperatures hinder sulfur (S) and phosphorus (P) removal, and excess carbon reduces carbon utilization efficiency. Optimal conditions are a carbon ratio of 0.2174 and a temperature of 1150 °C. The carbothermic reduction product requires further refinement through conventional ladle slag systems to meet the quality standards for metallic materials. Over 65% of alloying elements are recovered, though phosphorus content remains slightly higher than in finished alloy steel. The materials from this study are suitable as high‐quality intermediates for alloy steel production. [ABSTRACT FROM AUTHOR]

Bismuth-containing chromates, BixCrO1.5x+3 , were synthesized using a ceramic method from bismuth (III) and chromium (III) oxides, with a variable molar ratio of 1 ≤ n (Bi)/n (Cr) ≤ 38. The calcined samples exhibit a color variation from green to dark red, depending on the n (Bi)/n (Cr) ratio. The ceramic materials undergo a color change from green to red when a mixture of oxides with a significant predominance of bismuth oxide n (Bi2O3)/n (Cr2O3) ≥ 3 is subjected to a high-temperature treatment in air (at 650°C). It is noteworthy that the calcination of chromium (III) oxide under similar conditions occurs without the oxidation of chromium ions. X-ray diffraction analysis confirmed the formation of chromates, including Bi6Cr2O15, Bi10Cr2O21, Bi31Cr5O61.5, and Bi14CrO24. X-ray spectroscopy studies of the samples revealed that the NEXAFS Cr2p spectra of the red bismuth-chromium ceramics exhibited similarities in the main details of the K2CrO4 spectrum, indicating the presence of chromium in the oxide ceramics in the form of tetrahedral CrO 4 2 - ions. In addition, scanning electron microscopy data demonstrated that the samples exhibited a dense, low-porosity microstructure. [ABSTRACT FROM AUTHOR]

We report the detailed depth‐dependent structural and chemical analysis of the Cr2O3/Cr bilayer structure deposited on Si ˂100˃ substrate. The non‐destructive simultaneous X‐ray reflectivity and grazing incidence X‐ray fluorescence measurements were used for this purpose. Corresponding variation in the chemical state of Cr atoms as a function of depth has been studied using X‐ray standing wave (XSW) assisted X‐ray absorption near edge structure (XANES) measurements. Various oxidation states of Cr atoms present in the Cr2O3/Cr bilayer structure were determined using X‐ray photoelectron spectroscopy (XPS). Depth‐resolved XANES measurements confirmed the presence of chromium oxide (Cr2O3) and hydroxide (Cr (OH)3) at the top surface of the Cr2O3/Cr bilayer structure. The results also reveal the presence of metallic Cr along with its compounds Cr2O3 and Cr (OH)3 at the interface medium, showing significant mixing between the Cr2O3 and Cr layers. Our results clearly demonstrate that the XSW assisted XANES technique is extremely efficient for determining the variation of chemical states at the surface, interface, and different depths of a thin film structure. Such types of analysis are particularly useful for differentiating the presence of a metal from its own oxides, even at higher depths inside a thin film medium. [ABSTRACT FROM AUTHOR]

Corrosion behavior of (Cr2/3Ti1/3)3AlC2 and Ti3AlC2 in static oxygen‐saturated liquid lead–bismuth eutectic (LBE) at 550°C and (Cr2/3Ti1/3)3AlC2 in static oxygen‐depleted LBE at 500°C were investigated. In oxygen‐saturated corrosion, the loose and porous corrosion layer consisting of (PbTiO3 + TiO2) was generated on the surface of Ti3AlC2. In contrast, (Cr2/3Ti1/3)3AlC2 formed the protective Cr2O3 layer with better corrosion resistance. Moreover, dissolution corrosion of (Cr2/3Ti1/3)3AlC2 in oxygen‐depleted corrosion was intensified without a protective oxide film. And impurity phase TiC on the surface also caused the decomposition of matrix, thus impairing corrosion resistance. [ABSTRACT FROM AUTHOR]

In this work, Cr3+ ion introduced germanate transparent glass-ceramics with one-step heat treatment around the glass transition temperature were prepared. By using TEM and other structural characterizations, it was demonstrated that the microstructure of glass-ceramics had uniform distribution and excellent grain development. Through XPS, FTIR, Raman and JMA model calculation, it was found that the substitution of Cr 2 O 3 for Ga 2 O 3 led to the decrease of [TO 4 ] ratio in the glass network, and the crystallization behavior changed to the whole crystallization. The results of optical performance tests indicated that the transmittance of the transparent glass-ceramics with one-step heat treatment was 46 % higher than that of glass-ceramics prepared by the two-step heat treatment, and the broadband emission intensity at 980 nm was 1.69 times higher than that of the basic glass. There is some guiding relevance to the innovative preparation approach suggested in this work for the creation of transparent glass-ceramics. [ABSTRACT FROM AUTHOR]

The high-temperature shaping of steels is accompanied by the formation of surface scales composed of oxide layers. However, the oxidation kinetics and morphology of these scales remain poorly understood. This study analyses the formation of oxide layers on AISI 4140 steel at varying oxidation times (20, 40 and 60 min) at 1000 °C. The analysis revealed the presence of hematite, magnetite, and transformed wustite in the oxide layers, along with clusters of alloying element oxides, predominantly chromium and iron oxide (FeCr2O4). There was a direct correlation between the duration of the oxidation process and the thickness of the scale and the number of defects observed in the material. The coating layer of alloying element oxides demonstrated insufficient adhesion to the steel substrate. Similarly, the oxides of alloying elements within this layer exhibited low cohesion among themselves. The alloying elements are present in all oxide layers, but in greater quantity in the layer in contact with the steel substrate, where a reduction in their concentrations was observed over time. This indicates that the alloying elements tend to disperse as the thickness of the alloying element oxide layer increases over time. [ABSTRACT FROM AUTHOR]

The interfacial microstructure and corrosion behavior of oxide dispersion strengthening (ODS) FeCrAl alloy with 20 wt% Cr (e.g. 20Cr ODS FeCrAl alloy) exposed to static oxygen-saturated lead-bismuth eutectic (LBE) at 450 °C for 20 h, 40 h, 60 h, 80 h and 100 h as exposure time respectively have been investigated. The results show that multilayer corrosion films of 20Cr ODS FeCrAl alloy can exist at the corrosion interface. Due to formation of protective scales, the primary corrosion mechanism of 20Cr ODS FeCrAl alloy in LBE is oxidation rather than dissolution and penetration of liquid LBE. Specially, the spinel-shaped nano-sized dense external layer without any microcracks is obviously observed. Moreover, the dense and compact scale with micron-meters, i.e. Al-rich Fe-Cr spinel, generates at interface as the middle layer to effectively defend inward diffusion of oxygen and penetration of LBE. Meanwhile, a reinforced and continuous internal layer mixed with Cr2O3 scale and the ferrite inner oxidation zone (IOZ) existing in the form of the interlocking interface between the layers and the substrate can further promote the adhesion between corrosion layers and the substrate of 20Cr ODS FeCrAl. [ABSTRACT FROM AUTHOR]

In this article, the corrosion resistance of a cobalt–chromium‐based laser cladding reinforced with different microparticles: boron nitride, graphene oxide, and graphite, added for increased tribological performance, is explored. Samples are fabricated by premixing cobalt–chromium powder with microparticle additions and cladding onto 316L stainless steel base metal. The corrosion behavior is measured in industrially relevant applications: 1 m acetic acid and 3.5 wt% NaCl, using open‐circuit potential, electrochemical impedance spectroscopy, linear polarization resistance, and cyclic polarization. Laser ablation–inductively coupled plasma–mass spectrometry is used to analyze the distribution of the chemical elements throughout the coatings. The reference cladding's corrosion resistance is outstanding in both electrolytes, with a corrosion rate (CR) of ≤0.19 μm year−1 and no pitting tendencies. With the addition of microparticles, the claddings maintain their remarkable pitting resistance, but show an increase in CR up to 0.98 μm year−1 due to the nonuniform distribution of the microparticles into the matrix. [ABSTRACT FROM AUTHOR]

The combined effects of high‐temperature and long‐term exposure to oxidation environment on an AlCoCrFeNi‐based high entropy alloy (HEA) are investigated. The alloy has a composition of Al10Co20Cr20Fe20Ni30 (at%) and is oxidized in lab air at 1000 °C for 1000 h to emulate working conditions and long operation cycles of gas turbines. The microstructure and oxide formation of the HEA are characterized using scanning electron microscopy, energy‐dispersive spectroscopy, and X‐ray diffraction. The performance of the HEA is compared to that of Inconel 625 and Hastelloy X and shows slower oxidation kinetics than Inconel 625 until 750 h. The HEA has the thinnest oxide layer of the three alloys and exhibits a triplex structure with a continuous Cr2O3 outer scale, a semi‐continuous Al2O3 subscale, and deep AlN precipitates. The matrix shows signs of Cr and Al depletion after 1000 h, leading to its inability to replace the degraded oxide scales that evaporated or spalled, and decreases its long‐term oxidation resistance. Overall, the HEA shows good oxidation resistance until 750 h, but may benefit from a higher Al content on the surface to form a longer‐lasting Al2O3 subscale that would remain protective beyond 750 h. [ABSTRACT FROM AUTHOR]

Understanding of the hot corrosion behavior of each constitutive phase of the new Pt-enriched γ/γ′ nickel-based single-crystal TROPEA superalloy is of significant interest for further optimization. Therefore, single-phase γ and γ′ materials containing a low content of Pt (0.13% at.) were manufactured by inductive melting and their behavior was investigated at 900°C with 1 mg/cm2 of Na2SO4 deposit using thermogravimetry in air and air + 400 ppm of SO2. After 24 h in air, the scale grown on the γ′ model alloy consisted of an outer heterogeneous NiO layer and of an internal porous α-Al2O3 layer. The addition of 400 ppm of SO2 to air did not really change the nature and morphology of the oxides formed for γ′, but the measured linear rate was tenfold higher than that recorded in air. The γ alloy underwent an incubation period during which the corrosion rate was limited, followed by a propagation stage. In air, the alloy developed an external continuous NiCr2O4 spinel layer and a thin internal Cr2O3 subscale. The γ alloy was able to efficiently re-passivate after the propagation period. With 400 ppm SO2, only a thin protective layer Cr2O3 formed on the surface of γ, with large Cr2O3 crystals growing within the residual Na2SO4. The occurrence of Cr-rich sulfides was also greater in the γ′ model alloy compared to the γ counterpart both in air and in air + 400 ppm of SO2. Therefore, the results clearly evidenced the effect of SO2 on the type I hot corrosion. [ABSTRACT FROM AUTHOR]

The microstructure and oxidation resistance at 900 and 1000 °C of additively manufactured (AM) by directed energy deposition (DED) and conventionally manufactured (CM) Inconel 625 alloys were studied. The microstructure of the AM samples was cellular, with Nb and Mo segregations located in the dendritic and interdendritic regions. At 900 °C, the oxidation rate was similar for both materials, but was clearly higher for the AM material at 1000 °C, being related to the segregation and porosity present in the microstructure of the AM samples. Decrease in porosity by DED changing parameters allowed better oxidation resistance, but still considerably inferior than CM samples at 1000 °C. After oxidation, a layer of Cr2O3 was identified under all conditions, providing high resistance to oxidation. Internal oxidation of alumina was also observed in the CM and AM samples. The delta phase Ni3(Nb, Mo) was observed for the CM and AM alloys at the grain boundaries (900 °C) and at the metal/oxide interface for both temperatures as a result of chromium depletion. Finally, the oxide layer formed was compact and dense, and some voids were formed in the subsurface region of the samples produced by AM. [ABSTRACT FROM AUTHOR]

Samples of the Ni-based superalloy, RR1000, were exposed to 98% Na2SO4/2% NaCl salts at 700 °C with a flux of 1.5 µg cm−2 h−1 in flowing air + 300 ppm SO2 for a total of 250 h. Three pre-exposure conditions were studied: a bare reference alloy; fast heating to the test temperature followed by a 100 h hold; heating at a rate of 5 °C min−1 to the test temperature following by a 100 h hold. The surface oxide formed under the latter two conditions were Cr2O3 or NiCr2O4, respectively. The results show corrosion pit formation on the surface of the base, reference sample, and no pits present on the sample with the preformed Cr2O3. Some protection was found for the sample heated at 5 °C min−1 with a delay in the progression to accelerated corrosion attack. Additional testing under moisture containing air was also conducted. This showed no obvious difference in surface oxide morphology under the two tested heating rates for the short-term exposures examined but a difference was noted to be dependent on the moisture content of the air. [ABSTRACT FROM AUTHOR]

It is shown that studies of the coercivity of AFM domain walls that arise in antiferromagnets during the first-order spin-orientation transition can be used as a tool for detecting, identifying, and studying spin structures realized in a crystal under the influence of an external magnetic field. The use of high-frequency modulation of the magnetic field made it possible to expand the capabilities of the standard induction method of studying magnetic phase transitions in antiferromagnets. The proposed measurement method was tested on well-known MnF2 and Cr2O3 crystals. [ABSTRACT FROM AUTHOR]

In this paper, pre‐oxidation treatment was carried out at 950 °C under oxygen pressure of 10−16 atm for nickel‐10 % chromium‐x % aluminium‐1 % silicon‐0.5 % yttrium(x=0 wt.–%, 1 wt.–%, 3 wt.–%, 5 wt.–%) alloys. Morphology and structure of oxide layers on the alloys after pre‐oxidation were analyzed by scanning electron microscopy and electron discharge spectroscopy. The results showed that a chromium oxide film was formed on the surface of the alloy without aluminium addition, while the oxide layer on the surface of the alloy with aluminium addition gradually transformed into M2O3 (M=aluminium and chromium) oxide film. The oxidation behavior was analyzed by means of chemical thermodynamics, and it was seen that because the interaction coefficient,εijof aluminium and chromium is a positive value, the increase of aluminium addition will strengthen the interaction and increase the diffusion coefficient,Diof aluminium and chromium. The diffusion of chromium and aluminium in each other therefore promotes their interaction, which is beneficial to the formation of the outer oxide film. Thus, with the increase of aluminium addition, the thickness of the outer oxide film gradually increased, and the aluminium content in M2O3 (M=aluminium and chromium) increased significantly, and with 5 % aluminium added, the aluminium oxide of the outer oxide film became the main body. [ABSTRACT FROM AUTHOR]

CuM and AgM (M = Cr, Fe) catalysts were synthesized, characterized, and evaluated in methane reforming with CO2 with and without pretreatment under a H2 atmosphere. Their textural and structural characteristics were evaluated using various physicochemical methods, including XRD, B.E.T., SEM-EDS, XPS, and H2-TPR. It was shown that the nature of the species has a significant effect on these structural, textural, and reactivity properties. AgCr catalysts, presenting several oxidation states (Ag0, Ag+1, Cr3+, and Cr6+ in Ag, AgCrO2, and AgCr2O4), showed the most interesting catalytic performance in their composition. The intermediate Cr2O3 phase, formed during the catalytic reaction, played an important role as a catalytic precursor in the in situ production of highly dispersed nanoparticles, being less prone to coke formation in spite of the severe reaction conditions. In contrast, the AgFe catalyst showed low activity and a low selectivity for DRM in the explored temperature range, due to a significant contribution of the reverse water–gas shift reaction, which accounted for the low H2/CO ratios. [ABSTRACT FROM AUTHOR]

Simple Summary: Oleanolic acid is an organic natural compound, abundant in olive leaves, with various beneficial health effects in humans and animals. However, its in vivo efficacy is questioned given its low solubility, which hinders its bioavailability, that is, the capacity of a molecule to reach circulation. We investigated the digestibility and plasma concentration of oleanolic acid as an estimate of bioavailability in growing pigs. Because it is important to know the effects of oleanolic acid in the animal, growth, organ weights, digestibility of nutrients and plasma biochemical profile have been reported as well. Although there is a concern in the scientific community regarding the low bioavailability of oleanolic acid, in vivo data are lacking. We have demonstrated that, while digestibility of oleanolic acid was unexpectedly elevated, the appearance of the molecule in systemic blood was weak, probably indicating hepatic metabolism. No negative effects of oleanolic acid on growth or internal organs were observed. Oleanolic acid (OLA) has beneficial health effects in animals, but in vivo efficacy in monogastric animals is questioned due to its low bioavailability. To gain further insight on the nutritional effects of OLA it was administered as part of a diet. We investigated digestibility and plasma OLA in pigs and the associated influence on growth, organs, digestibility of nutrients and plasma biochemical profile. Twenty-four crossbred barrows (23.7 ± 1.0 kg BW) were assigned one of three treatments: Control (basal diet without OLA), OLA-1 (basal diet with 260 mg/free OLA) and OLA-2 (basal diet with 260 mg/kg cyclodextrin-OLA). Diets included chromium oxide to estimate digestibility. Blood samples were collected on day 14 for OLA analysis and feces on days 22–24 for determining digestibility. Pigs were slaughtered on day 31 (39.9 ± 2.43 kg BW) and their blood collected for analysis. Growth and organ weights were not affected (p > 0.05). OLA-1 decreased apparent total tract digestibility (ATTD) of energy (p < 0.05). OLA-2 increased ATTD of dry and organic matter compared with Control pigs (p < 0.05). OLA-1 increased plasma calcium and alkaline phosphatase (p < 0.05). Ileal digestibility of OLA was not affected (0.88), although OLA ATTD increased in OLA-1 compared to Control pigs (0.75 vs. 0.82; p < 0.05). OLA-1 and OLA-2 increased plasma OLA compared to Control pigs (p < 0.05 and p = 0.083). In conclusion, although the OLA was digested and absorbed, plasma concentration was low (4.29 µg/L), and pig growth, organs and plasma parameters were not affected. [ABSTRACT FROM AUTHOR]

In this study, we optimized the traditional composition of AISI 8630 steel and evaluated its corrosion resistance through a series of tests. We conducted corrosion tests in a 3.5% NaCl solution and performed a 720 h fixed-load tensile test in accordance with the NACE TM-0177-2016 standard to assess sulfide stress corrosion cracking (SSCC). To analyze the corrosion products and the structure of the corrosion film, we employed X-ray diffraction and transmission electron microscopy. The corrosion rate, characteristics of the corrosion products, structure of the corrosion film, and corrosion resistance mechanism of the material were investigated. The results indicate that the optimized AISI 8630 material demonstrates excellent corrosion resistance. After 720 h of exposure, the primary corrosion products were identified as chromium oxide, copper sulfide, iron oxide, and iron–nickel sulfide. The corrosion film exhibited a three-layer structure: the innermost layer with a thickness of 200–300 nm contained higher concentrations of alloying elements and formed a dense, cohesive rust layer that hindered the diffusion of oxygen and chloride ions, thus enhancing corrosion resistance. The middle layer was thicker and less rich in alloying elements, while the outer layer, approximately 300–400 nm thick, was relatively loose. [ABSTRACT FROM AUTHOR]

The influence of chromium‐bearing filler sand on the transformation of inclusions in high‐Mn and high‐Al steel under various reaction times and Mn content levels is studied, and the mechanism of filler sand intrusion into the steel matrix is analyzed. It is demonstrated that an inclusion containing Cr2O3 is discovered. The evolution pathway of oxide inclusions is identified as Al2O3–MnO → Al2O3–MnO–SiO2 → Al2O3–MnO–SiO2–Cr2O3(Cr2O3 + MnO–SiO2) → Al2O3–MnO–Cr2O3–MgO·Al2O3. It is noteworthy that Cr2O3 inclusions tend to diffuse from the outside inward, but the internal content remains almost unchanged, which is due to the strong diffusion hindrance of SiO2. The formation of a liquid phase in the filler sand is a necessary condition for its infiltration into the steel matrix. The critical liquid‐phase content that results in the formation of Cr2O3 inclusions is 42%, which contains 5–8% of Cr2O3. The formation of pore channels provides favorable conditions for sand penetration, with the maximum penetration depth reaching up to 29 mm. Large sand inclusion particles reach millimeter scale in size and are distributed quite randomly. Chemical reactions at the steel/sand interface can lead to an increase in the total oxygen (T.O) content in the steel. The reaction time has little effect on the T.O content, while the Mn content in the steel has a significant impact, with an increase of up to 41 ppm. During the smelting stage, the filler sand can enter the molten steel, thereby affecting the quality of the product. [ABSTRACT FROM AUTHOR]

Incorporation of MAX phase to fabricate low-carbon refractories has been recently proposed. Among them, Cr 2 AlC was the undoubtedly one which was regarded as the most potential candidates for applications, due to the excellent chemical stability of chromium oxide. In this work, the influence of Cr 2 AlC on the thermal shock resistance and corrosion resistance of Al 2 O 3 -Cr 2 AlC-C refractories were investigated. The results indicated that the residual strength ratio still maintained stability when flake graphite content reduced from 9 wt% to 4 wt%. While the corrosion resistance of the sample with 4 wt% graphite and 5 wt% Cr 2 AlC increased approximately 40% compared with regular Al 2 O 3 -C refractories with 9 wt% graphite. The degradation mechanisms and interactions of Al 2 O 3 -Cr 2 AlC-C refractories in contact with MnO-rich slag were studied, and the role of Cr 2 AlC was elucidated. [ABSTRACT FROM AUTHOR]

A series of Cr 2− x Fe x O 3 (0.0 ≤ x ≤ 0.3) nanoparticles were successfully synthesized using a sol-gel-based method. Analysis through XRD and SAED of both pure and Fe-doped Cr 2 O 3 nanoparticles revealed a rhombohedral structure belonging to the R 3 ‾ c D 3 d 6 space group, without the formation of secondary phases or Fe clusters. Fe ions were well integrated, as indicated by fluctuations in lattice parameters, and lattice strain. The crystallite size decreased from 38.42 to 27.54 nm with increasing doping concentration. HRTEM images depicted evenly distributed nanoparticles. At lower dopant concentrations (x = 0.1), smaller and more heterogeneous nanorod-like structures emerged, with average sizes and lengths of 36.56 and 39 nm, respectively. Increasing the doping content to x = 0.2 resulted in a morphological shift towards semi-spherical and ellipsoidal shapes, with average dimensions of 22.84 and 31 nm, respectively. At higher doping levels (x = 0.3), nanoparticles grew to 66.5 nm in size and exhibited a spherical morphology. Raman and Fourier transform infrared spectra showed red-shifting of absorption bands with increasing Fe content, attributed to variations in bond length and Cr/Fe–O–Cr/Fe structural perturbation. XPS and Mössbauer spectroscopy analyses confirmed the oxidation states of Fe3+ and ionized oxygen vacancies in the crystal lattice of Cr 2 O 3 nanoparticles. Higher values of quadrupolar splitting Δ indicated greater structural disorder induced by Fe3+ in octahedral positions and in an oxygen-deficient environment. Atomistic simulations confirmed that Fe3+ dopants can induce the presence of vacancy-complexes, forming a stable double-defect configuration with vacant Cr sites along the c-axis, proximal to oxygen vacancies with a single positive charge. These findings offer both experimental and theoretical insights into the dynamics of structural defects in trivalent transition metal doping of Cr 2 O 3 nanoparticles, which holds significant implications for spintronics research. [ABSTRACT FROM AUTHOR]

The superior anti-oxidation layer induced by the PVA-boehmite sol-gel film on the AISI304 steel during the cyclic oxidation is investigated in this work. The moderate PVA addition in the boehmite sol conduces to increase the film thickness and is beneficial to the adhesion between the film and the substrate. The presence of the PVA-boehmite film leads to a significant reduction in mass gain during the high-temperature cyclic oxidation at 800 °C, demonstrating the enhanced oxidation resistance. The generated oxide layer induced by the PVA-boehmite film presents as a thin, compact, and continuous layer without spalling, offering sustainable protection against oxidation etching. The PVA-boehmite film promotes the preferential formation of the corundum (Al, Cr) 2 O 3 phase rather than the detrimental hematite Fe 2 O 3 phase during the oxidation procedure, which facilitates the development of the above compact oxide layer. Finally, the superior anti-oxidation oxide layer is characterized as a novel dual-layer structure: the outer spinel MnCr 2 O 4 layer and the inner corundum (Al, Cr) 2 O 3 layer, effectively delaying the oxidation process. [ABSTRACT FROM AUTHOR]

High entropy oxides (HEOs) have garnered much interest due to their available high degree of tunability. Here, we study the local structure of (MgNiCuCoZn)0.167(MnCr)0.083O, a composition based on the parent HEO (MgNiCuCoZn)0.2O. We synthesized a series of thin films via pulsed laser deposition at incremental oxygen partial pressures. X‐ray diffraction shows lattice parameters to decrease with increased pO2 pressures until the onset of phase separation. X‐ray absorption fine structure shows that specific atomic species in the composition dictate the global structure of the material as Cr, Co, and Mn shift to energetically favorable coordination with increasing pressure. Transmission electron microscopy analysis on a lower‐pressure sample exhibits a rock salt structure, but the higher‐pressure sample reveals reflections reminiscent of the spinel structure. In all, these findings give a more complete picture of how (MgNiCuCoZn)0.167(MnCr)0.083O forms with varying initial conditions and advances fundamental knowledge of cation behavior in high entropy oxides. [ABSTRACT FROM AUTHOR]

In the present study, the origin of three energy gaps of lanthanum chromium oxide, one arises due to the charge-transfer gap between O-2p and Cr-3d and two arises from the d–d transitions, is analyzed in detail using the diffuse reflectance spectroscopy technique. The spin allowed transitions, such as 4T1(P)→4A2, 4T1(F)→4A2, and 4T2→4A2, and the spin and parity forbidden 2E →4A2 transitions are depicted using a Tanabe–Sugano (T–S) diagram and an absorption spectrum. The high crystal field strength of 3.27 obtained from the T–S diagram provides high directional emission and makes the system suitable for near infrared lasing applications. Moreover, the investigations into the variation of a charge-transfer gap with temperature will provide insights into the modification of numerous optical properties toward development of optoelectronic devices. Using this temperature-dependent diffuse reflectance spectroscopy studies, we have obtained the important optical parameters, such as Urbach energy (Eu) and Urbach focus. Furthermore, first-principles calculations are carried out in order to validate the experimental findings on LaCrO3. The experimental results are in consonance with the charge-transfer gap obtained from the theoretical calculations. Furthermore, the bandgap variation with temperature is fitted using Varshni's relation, and the Debye temperature is calculated. [ABSTRACT FROM AUTHOR]

Magnetic graphene hybrid has encouraging application in environmental remediation. Herein, adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -graphene oxide (Fe 3 O 4 -GO) surface was inspected via both theoretical and experimental methods. In the theoretical level, acidity impact on Cr (Ⅵ) species evolution and Cr (Ⅵ)→Cr (Ⅲ) reduction was investigated with the methodology of equilibrium thermodynamics. In the experimental level, adsorption fittings and spectroscopic tests (FTIR, UV–Vis, XPS) were performed to clarify the adsorbent-adsorbate interaction. Results indicate: (1) Under acidic condition, Cr (Ⅵ) is adsorbed by Fe 3 O 4 -GO in the form of H 2 CrO 4. Afterwards, over three-fifths of H 2 CrO 4 is reduced to Cr (Ⅲ), reaching adsorption percent and quantity 95.53 % and 382.10 mg g−1 in 10 min (2) Under basic condition, Cr (Ⅵ) is adsorbed in the form of CrO 4 2− without reduction. In the context of environmental remediation, two special implications are thereby procured. (1) Under acidic condition, Cr (Ⅵ) removal efficiency at the first cycle is maximized, while magnetic recovery is deteriorated, resulting in unsatisfactory cyclic performance. (2) Under basic condition, Cr (Ⅵ) removal efficiency is inferior to that under acidic condition, while magnetic recovery is guaranteed, leading to satisfactory cyclic performance. Exploration of this work provides reference especially for developing Fe 3 O 4 -GO architecture towards efficient sequestering of hexavalent chromium. Adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -GO surface(a) Illumination of redox reaction between Cr (Ⅵ) and Fe 3 O 4 given by thermodynamic calculation. Under acidic condition: spontaneous reaction H2CrO4+3Fe 2+ +6H + ⇌Cr 3+ +3Fe 3+ +4H2O owing to highly negative standard molar Gibbs free energy change. Under basic condition, non spontaneous reaction CrO4 2− +3Fe 2+ +4H2O⇌Cr(OH)4 - +3Fe 3+ +4OH − owing to highly positive standard molar Gibbs free energy change. (b) Adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -GO surface deciphered by Cr (Ⅵ) species distribution and XPS test. Under acidic condition: five small orange balls symbolizing H 2 CrO 4 adsorbed onto the surface of the big green ball representing Fe 3 O 4 -GO. Subsequently, three out of five small orange balls were transformed into small violet balls representing Cr3+, approaching the molar ratio Cr (Ⅲ)/Cr (Ⅵ) = 1.52 of the sample Fe 3 O 4 -GO-Cr as determined by XPS test (Fig. 8). The big blue ball represents Fe 3 O 4 -GO oxidized by H 2 CrO 4. Under basic condition: five small pink balls symbolizing CrO 4 2− adsorbed onto the surface of the big green ball representing Fe 3 O 4 -GO ensued by no reduction, as confirmed by thermodynamic analysis. [Display omitted] • Adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -graphene oxide surface is inspected. • In acidic media, H 2 CrO 4 is adsorbed, three-fifths of which is reduced to Cr (Ⅲ). • In basic media, CrO 4 2− is adsorbed without reduction. • Superior Cr (Ⅵ) removal efficiency but unsatisfactory cyclic performance in acidic media. [ABSTRACT FROM AUTHOR]

The oxidation of six NbTi-i refractory medium- and high-entropy alloys (NbTi + Ta, NbTi + CrTa, NbTi + AlTa, NbTi + AlMo, NbTi + AlMoTa and NbTi + AlCrMo) were investigated at 1000 °C for 20 h. According to our observation, increased Cr content promoted the formation of protective CrNbO4 and Cr2O3 oxides in NbTi + CrTa and NbTi + AlCrMo, enhancing oxidation resistance. The addition of Al resulted in the formation of AlTi-rich oxide in NbTi + AlTa. Ta addition resulted in the formation of complex oxides (MoTiTa8O25 and TiTaO4) and decreased oxidation resistance. Meanwhile, Mo's low oxygen solubility could be beneficial for oxidation resistance while protective Cr2O3/CrNbO4 layers were formed. In NbTi + Ta, NbTi + AlTa and NbTi + CrTa, a considerable quantity of Ti-rich oxide was observed at the interdendritic region. In NbTi + AlCrMo, the enrichment of Cr and Ti at the interdendritic region could fasten the rate of oxidation. Compared to the recent research, NbTi + AlCrMo alloy is a light-weight oxidation-resistant alloy (weight gain of 1.29 mg/cm2 at 1000 °C for 20 h and low density (7.2 g/cm3)). [ABSTRACT FROM AUTHOR]

This article uses a high-temperature sintering imaging instrument to test the flowability of borosilicate glass melt doped with Cr 2 O 3 , and establishes a mathematical model for high-temperature glass melt spreading. Discuss the glass melt from a thermodynamic perspective by combining model interpretation with experimental characterization. The results indicate that the thermodynamic judgment formula for high-temperature flow spreading of borosilicate glass is: Q ≥ ρ [ A 0 exp (− T / k 0) + S 0 ] − M · δ [ A 0 exp (− T / k 0) + S 0 ] 1 / 2 . To improve the high-temperature flow ability of borosilicate glass, it is necessary to increase the spreading activation energy Q. On the other hand, it is necessary to reduce the spreading coefficients A 0 、 k 0 and S 0. As a refractory metal oxide and active oxide, Cr 2 O 3 plays a role in reducing the spreading coefficient of glass systems. [ABSTRACT FROM AUTHOR]

Simple Summary: Defatting can be performed mechanically by cutting the frozen insect larvae and then pressing them to enable the leakage of intracellular fat, or chemically using petroleum ether extraction of the insect meal. This study aimed to investigate the effects of different defatting methods of black soldier fly (Hermetia illucens) larvae meal (BSFM) on the metabolic energy and nutrient digestibility in laying hens. The results show that both defatting methods of BSFM had no adverse effects on the metabolic energy and nutrient digestibility in young laying hens, but pressed black soldier fly meal (BSFMp) demonstrated better effects on the digestibility of metabolic energy and nutrients in the feed for young laying hens. This study aimed to investigate the effects of different defatting methods of black soldier fly (Hermetia illucens) larvae meal (BSFM) on the metabolic energy and nutrient digestibility in laying hens. Sixty young laying hens (Hy-Line W-36) aged 63 days were randomly divided into two groups (G1 and G2), each with five replicates of six hens housed in individual cages. Group G1 was fed 25% pressed black soldier fly meal (BSFMp) and 75% basal diet, and Group G2 was fed 25% extracted black soldier fly meal (BSFMe) and a 75% basal diet. Both diets included 5 g/kg chromium oxide as an external marker. A 7-day preliminary trial was followed by a 4-day experimental period. The results indicate that pressing and extracting significantly affected the digestibility of crude fat and total energy in BSFM, with BSFMp showing significantly higher crude fat digestibility than BSFMe. Similarly, total energy digestibility was also significantly higher in BSFMp. However, there were no significant differences in dry matter, organic matter, and crude protein digestibility between the two processing methods. The apparent metabolic energy values of BSFMp and BSFMe were 16.34 and 12.41 MJ/kg, respectively, showing a significant difference. The nitrogen-corrected metabolic energy values were 15.89 MJ/kg in BSFMp and 11.93 MJ/kg in BSFMe, indicating a highly significant difference. The digestibility of arginine and leucine in BSFMp was significantly higher than in BSFMe, while differences in lysine, cystine, threonine, tryptophan, and isoleucine were not significant. In conclusion, both defatting methods of BSFM had no adverse effects on the metabolic energy and nutrient digestibility in young laying hens, but BSFMp demonstrated better effects on the digestibility of metabolic energy and nutrients in the feed for young laying hens. [ABSTRACT FROM AUTHOR]

Thin buried magnetic layers ranging from thicknesses of a few atomic monolayers to several nanometers are omnipresent in the fields of magnetism and spintronics. For the functionality and fine tuning of devices build with such layers, exact knowledge of the depth dependent magnetic properties is essential. Especially the interfacial magnetic properties are important. Hence, understanding how magnetism is affected by structural variations, such as thickness or interface roughness, is mandatory. In this study, we use x-ray resonant magnetic reflectometry and magnetometry to study the high-resolution depth dependent magnetization profiles of thin magnetic transition metal layers sandwiched between an oxide and chromium layer. Compared to bulk materials, the room temperature saturation magnetization of these layers is reduced by up to 67%. These reductions are extremely sensitive to small structural variations. From the magnetic depth profiles, we disentangle different effects contributing to the magnetization reduction and the exact magnetic properties of the interface. [ABSTRACT FROM AUTHOR]

The document is a contents list for the New Journal of Chemistry, a journal focused on new directions in chemistry. It includes various articles and papers on topics such as lithium-ion batteries, organic synthesis, photocatalysts, and nanocatalytic systems. The journal is published by The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. [Extracted from the article]

The conversion of CO2 into liquid fuels, using only sunlight and water, offers a promising path to carbon neutrality. An outstanding challenge is to achieve high efficiency and product selectivity. Here, we introduce a wireless photocatalytic architecture for conversion of CO2 and water into methanol and oxygen. The catalytic material consists of semiconducting nanowires decorated with core-shell nanoparticles, with a copper-rhodium core and a chromium oxide shell. The Rh/CrOOH interface provides a unidirectional channel for proton reduction, enabling hydrogen spillover at the core-shell interface. The vectorial transfer of protons, electrons, and hydrogen atoms allows for switching the mechanism of CO2 reduction from a proton-coupled electron transfer pathway in aqueous solution to hydrogenation of CO2 with a solar-to-methanol efficiency of 0.22%. The reported findings demonstrate a highly efficient, stable, and scalable wireless system for synthesis of methanol from CO2 that could provide a viable path toward carbon neutrality and environmental sustainability. [ABSTRACT FROM AUTHOR]

This study investigates the effects of using biodiesel from Mesua ferrea (BD20) and chromium oxide (Cr2O3) nanoparticles in diesel engines. The Response Surface Methodology (RSM) model and artificial neural networks (ANNs) were developed to make precise predictions of the operating parameters. The amount of Cr2O3 nanoparticles was set at 80 mg/L, and surfactant and dispersant were applied to the nanoparticles in the same amounts. The study was carried out with different compression ratios and load conditions. The parameters evaluated were engine load, fuel samples and compression ratio as inputs and BTE, BSFC, CP, NHRR, CO, UHC, NO x and smoke opacity as outputs. The addition of the QPAN80 additive at the same dosage of 80 mg/L together with the BD20 fuel blend containing Cr2O3 at a concentration of 80 mg/L resulted in a significant increase in BTE by 16.58 % and a reduction in BSFC by 0.58 %. While the NHRR increased by 85.40 %, the CP increased sharply by 24.47 %. The CO concentration decreased by 31.85 %, the UHC concentration by 22.22 %, the NO x concentration by 6.16 % and the smoke emission by 62.61 %. For each output parameter, the correlation coefficient (R 2), calculated using ANNs and RSM was between 0.96 and 0.98. The observed range of values demonstrates a robust correlation between the experimental data and the predicted outcomes. [ABSTRACT FROM AUTHOR]

Zirconia-toughened alumina (ZTA) ceramics have attracted much attention in the medical field as joint replacement materials due to their good mechanical properties and biocompatibility. However, the flexural strength of conventional ZTA is still slightly insufficient in traditional preparation techniques. In this study, by improving the slurry system, the effects of the solid content of the slurry, additives, and the pH of the slurry on the slurry system were investigated. ZTA powders with a uniform particle size distribution, high degree of sphericity and high flowability were prepared by spray granulation. The mechanical properties, microstructure and biocompatibility of the ZTA pressing were investigated after degreasing and sintering processes. The results showed that the hardness of the prepared ZTA ceramics was 1658.24 ± 28.04 H V, the fracture toughness was 4.016 ± 0.027 MPa m1/2, and the biaxial bending strength was 501.43 ± 21.44 MPa, and the three-point bending strength reached 635 MPa. The ZTA ceramics also possessed good biocompatibility and a low haemolysis rate, which aligns with the requirements of clinical biomedical implant materials. [ABSTRACT FROM AUTHOR]

CrN/TiSiN multilayer coatings deposited at 316 L substrate were selected to explore the effects of irradiation on LBE (Liquid Pb–Bi eutectic alloy) corrosion. The as-deposited and irradiated coatings were exposed in LBE. After exposure, all CrN/TiSiN coatings presented oxidation accompanied with PbBi penetration. Irradiated coatings revealed better corrosion resistance with thinner oxide layer and smaller penetration thickness. The largest decrement of 39 % in oxidation thickness was observed in CrN/TiSiN deposited with Ti 80 Si 20 under 150 V. The irradiation-decelerated LBE corrosion could be attributed to the rapidly formed protective oxide layer resulting from the irradiation defects which accelerated nucleation and diffusion process during oxides formation. The decelerated effect was relatively weak in coatings deposited with a bias voltage under 100 V, in which the decrement is under 10 %. The enhanced corrosion resistance was attributed to the quickly formed dense and continuous chromium oxide which rapidly formed due to the irradiation induced defects and acted as diffusion barrier to slow down LBE penetration. [ABSTRACT FROM AUTHOR]

In this study, pure iron, S45C carbon steel (Fe–0.45mass%C), carburized iron, and nitrided iron are bonded with two types of stainless steels, i.e., SUS304 austenitic stainless steel (Fe–18mass%Cr–8mass%Ni) with face center cubic structure or SUS430 ferritic stainless steel (Fe–18mass%Cr) with body center cubic structure by a spark plasma sintering (SPS) machine. Bonding experiments are carried out by SPS bonding. It is found that the bonding temperature of the S45C/SUS samples is lower than that of Fe/SUS samples, and carbon atoms in the S45C play important role on the bonding performance. The bonding temperature for SUS304/SUS430 sample is more than 30 °C higher than those for the Fe/SUS and S45C/SUS samples. The presence of thin chromium oxides on both stainless steels reduces the bonding performance of SUS304/SUS430 sample. Better bonding performance is found for the carburized and nitrided iron for bonding with stainless steels. However, continuous single‐phase layer on the surface leads to reduce the bonding performance. It is concluded that not only the concentration of carbon and nitrogen but also the phase configuration in the iron at interface strongly influences the bonding performance between iron alloys and stainless steels by SPS bonding. [ABSTRACT FROM AUTHOR]

The new ludwigite-group mineral savelievaite, ideally Mg2Cr3+O2(BO3), was found in the chromitite body at the Malaya Kharamatalou river valley, Voikar–Syninskiy ultrabasic complex, Polar Urals, Russia. Savelievaite and Cr-enriched ludwigite occur in clinochlore veinlets and are associated with earlier magnesiochromite, spinel, chromite, pargasite, diopside, forsterite, serpentine, magnetite and pentlandite. Savelievaite forms prismatic, acicular or fibrous crystals up to 0.05 × 0.4 mm, usually assembled in radiating or chaotic clusters up to 1 × 1.5 mm across. It is opaque, black to greenish-black. The lustre is vitreous for prismatic crystals and silky for fibrous aggregates. D (calc.) = 3.91 g cm–3. Under the microscope in reflected light, savelievaite is grey, non-pleochroic, with weak bireflectance and anisotropism. The chemical composition (wt.%, EMPA, Fe2+:Fe3+ ratio by stoichiometry) is: MgO 34.88, FeO 10.83, NiO 0.36, B2O3 16.80, Al2O3 2.97, V2O3 0.21, Cr2O3 21.97, Fe2O3 12.40, TiO2 0.43, total 100.85. The empirical formula calculated on the basis of 5 O apfu is (Mg1.72Fe2+0.30Ni0.01)Σ2.03(Cr3+0.57Fe3+0.31Al0.12Ti0.01V3+0.01)Σ1.02B0.96O5. Savelievaite is orthorhombic, space group Pbam , a = 9.2631(6), b = 12.2298(8), c = 3.0104(2) Å, V = 341.04(4) Å3 and Z = 4. The strongest reflections of the powder X-ray diffraction pattern [ d ,Å(I)(hkl)] are: 5.101(100)(120); 2.551(90)(240); 2.524(88)(201); 2.163(36)(250); and 2.033(55)(321). The crystal structure was solved from single-crystal X-ray diffraction data and refined to R 1 = 0.0405. Savelievaite is isostructural with ludwigite, Cr3+ is concentrated at the M 4 site. The mineral is named in honour of the Russian petrologist and geologist Dr. Galina Nikolaevna Savelieva (b. 1936). Ludwigite, ideally Mg2Fe3+O2(BO3), and savelievaite form a continuous isomorphous series in which Cr3+ content varies from 0 to 0.60 apfu. Occurrences of Cr-enriched (>1 wt.% Cr2O3) varieties of ludwigite are mainly related to ultrabasic complexes. The Cr-richest (>10 wt.% Cr2O3) ludwigite–savelievaite-series members are found in chromite ores at the Voikar–Syninskiy complex and Volchiegorskoe and Tatishchevskoe deposits, both in the South Urals. [ABSTRACT FROM AUTHOR]

It aimed to estimate the forage intake by lambs managed in different leaf allowances on Brachiaria-grass using internal and external markers. Forty-eight Texel lambs with 17.52 ± 3.48 kg were evaluated which were 12 testers and 36 regulators. The lambs were kept in twelve paddocks, subdivided into four treatments based on green leaf allowance (60, 75, 90, and 105 g/kg of BW). The experimental design was completely randomised. To estimate dry matter intake (DMI), the following markers were used: indigestible dry matter (iDM); indigestible neutral detergent fibre (iNDF); indigestible acid detergent fibre (iADF); lignin in indigestible acid detergent (iADL) and titanium dioxide (TiO2). Comparisons between intake markers were made using Chromic Oxide (Cr2O3) as a control marker. The leaves allowance tested did not alter the voluntary intake by lambs kept in Brachiaria-grass pasture. Comparison between the control intake marker (Cr2O3) and the other markers by Dunnett's test showed that, regardless of green leaf allowance, the Cr2O3, TiO2 and iADL markers provided similar estimates of DMI, but with lower values than the other markers. External marker TiO2 and the internal iADL were demonstrated to be more suitable for estimating the dry matter intake in grazing lambs regardless of the leaf allowance. [ABSTRACT FROM AUTHOR]

The cyclic oxidation behavior of an additive manufactured CoCrMo alloy with 0.14 wt.% C was investigated at 914 °C for 32 cycles, each lasting 10 h, resulting in a total exposure time of 320 h. The oxidation rate was assessed for mass gain after finishing each 40 h oxidation cycle. It was experimentally determined that the oxidative process at 914 °C of this CoCrMo alloy follows a parabolic law, with the process being fast at the beginning and slowing down after the first 40 h. The microstructural analysis revealed that in the as-printed state, the phases developed were primarily the γ matrix and minor traces of ε phase. The oxidative process ensured an increase in the ε phase and precipitation of carbides which produced a 12% increase in the material's hardness after the first 40 h of exposure at 914 °C. The oxidation process led to the development of an oxide scale comprising a dense Cr2O3 layer and a porous layer of CoCr2O4 spinel, the latter spalling after the 240 h of exposure. Despite this spallation, the oxide scale continued to develop in the presence of O, Cr, and Co. The experimental analysis provided valuable insights regarding the material's behavior under prolonged exposure at high temperature in air, demonstrating its suitability as a candidate for additive manufactured mandrels used for bending metallic pipe fitting elbows. [ABSTRACT FROM AUTHOR]

The podiform chromitites in the Luobusha ophiolite have been thought to experience a very deep formation, but the maximum depth is still an open issue. Here, we have investigated the structural stability of natural magnesiochromite using the synchrotron-based powder X-ray diffraction and diamond anvil cells up to 48.6 GPa and 2 450 K. The results have shown that spinel-type magnesiochromite first decomposes into corundum-type 'Cr2O3' + B1-type 'MgO' at 11–14 GPa and 1 250–1 450 K, then modified ludwigite (mLd)-type 'Mg2Cr2O5' + corundum-type 'Cr2O3' at 14.3–20.5 GPa and 1 300–2 000 K, and finally CaTi2O4-type phase at 24.5 GPa. During the quenching procession from high-temperature-pressure conditions, the mLd-type phase appeared again and was kept at ambient conditions. We also obtained the isothermal equation states of spinel-type and CaTi2O4-type phases, revealing the composition effect on their elasticities. Based on the updated results, we propose chromitites could not experience pressure exceeding ∼14.3 GPa (approximate maximum depth ∼400 km) in the subduction-recycling genesis model. [ABSTRACT FROM AUTHOR]

Aiming to address the Mo volatilization problem of super-austenitic stainless steel at high temperature, the S31254 steel containing B and rare earth element Y with high oxidation resistance was designed. It was observed that a synergy of B + Y can promote the formation of the dense Cr2O3 layer at 1050 and 1100 °C, making MoO3 layer formation difficult. While the oxide layers of the 0B sample from top to bottom were divided into four layers: Fe-rich oxide layer, MoO3 layer, Cr–Mn–Ni spinel oxide layer, and Cr2O3 layer (loose and porous), thus the undense Cr2O3 layer in the 0B sample can hardly inhibit MoO3 volatilization, especially at 1100 °C. In addition, the synergistic effect of B and Y on the diffusion of Cr to the surface was calculated using first-principles calculations. The results demonstrated that both the addition of B and Y can enhance Cr diffusion to the surface, while Y can specifically promote the combination of Cr and O. Consequently, the combined presence of B and Y exhibits a more favorable synergy for improving the density of the Cr2O3 layer, effectively inhibiting MoO3 formation and volatilization, thereby enhancing the oxidation resistance of S31254. [ABSTRACT FROM AUTHOR]