High Cr Research Articles

Exploring the Influence of Food Culture Attributes on Visitor Satisfaction and Motivations at Food Festivals

This study examines the impact of food culture aspects such as taste, display, and preparation process on visitor satisfaction and motivation during food festivals. Data from 150 participants were analyzed utilizing SPSS 25 for data analysis. The study uses Spearman's Rank Correlation, Confirmatory Factor Analysis (CFA), and Chi-Square testing to investigate how these characteristics influence festival experiences. Significant positive correlations were found using Spearman's Rank Correlation, taste had a strong correlation with visitor satisfaction (ρ = 0.65,p = 0.01) and motivation (ρ = 0.60,p = 0.02), while display also had a moderately positive correlation with both (ρ = 0.55,p = 0.05) satisfaction and motivation (ρ = 0.50,p = 0.04). The association for the preparation process, however, was not statistically significant and was much weaker. It was established that CFA had high dependability with estimates of 0.78 for taste, 0.85 for display, and 0.80 for the preparation procedure, all of which met high CR and AVE values. The relationships between aspects of food culture and visitor outcomes were evaluated using the Chi-Square Test. Taste was found to have significant correlations with motivation (χ² = 10.45, p = 0.05) and satisfaction. While the display was only significantly connected with satisfaction (χ² = 7.89, p = 0.10), the preparation process was strongly associated with satisfaction (χ² = 12.34, p = 0.03). These results emphasize how important taste is to improving visitor experiences and show how particular characteristics of food cultures can affect festivalgoers' motivation and level of satisfaction. The study found that taste has a substantial impact on both satisfaction and motivation, emphasizing its importance for good event planning and increased attendee involvement.

Studies on fuels and engine attributes powered by bio-diesel and bio-oil derived from stone apple seed (Aegle marmelos) for bioenergy

Biofuel is an alternative fuel for diesel engines which is necessary to reduce exhaust emissions and helps to balance the depletion of fossil fuels. This study details the synthesis of bio-diesel and bio-oil from stone apple seeds ( Aegle marmelos) through transesterification, direct oxygenate additive, and pyrolysis processes. The diesel engine is powered by the resulting stone apple methyl ester bio-diesel/diesel and bio-oil/diesel mixtures. In a test engine rig, the effectiveness and emission uniqueness of test fuel mixes were examined at various engine loads (EL = 3 kg–12 kg) and compression ratios (CR = 16–17.5) while maintaining a steady speed of 1500 r/min. Furthermore, engine performance and emissions for bio-diesel and bio-oil are measured and compared. The oxides of nitrogen (NOx) emission by bio-diesel and bio-oil opus were higher than neat diesel (FD). Also, carbon monoxide (CO) and hydrocarbon (HC) emissions were measured to be lower. The improvements of BTE by 4.87% and decrement of CO by 18.8%, HC by 13.26% were observed with the trans-esterified bio-diesel/diesel opus compared to diesel at a higher CR and rated load conditions. The engine analysis responses revealed that the FBD blend showed enhanced performance and lower emissions except NOx compared to diesel fuel. Hence, trans-esterified bio-diesel is a greater diesel alternative than FBDE and FBO.

Retrieval of chromium and mercury concentrations in agricultural soils: Using spectral information, environmental covariates, or a fusion of both?

The universal contamination of arable land with potentially toxic elements (PTEs) poses a severe threat to food security and jeopardizes worldwide efforts to meet the United Nations Sustainable Development Goals (SDGs). How to obtain more reliable concentrations of PTEs in regional agricultural soils is a priority problem to be solved. Multispectral satellite remote sensing, with its advantages of high spatial and temporal resolution, broad coverage, and low cost, offers the potential to acquire spatial distribution of PTEs in agricultural soils over large areas. However, owing to the complexity of soil environments and the insufficiency of spectral information, the mechanism for retrieving concentrations of PTEs in agricultural soils via multispectral satellites is not yet clear, and the accuracy needs to be improved. In this study, we aimed to assess whether employing a fusion of spectral information and environmental covariates, results in more accurate retrievals of PTEs, specifically chromium (Cr) and mercury (Hg), in croplands than does employing spectral information alone. Three machine learning algorithms—kernel-based support vector machine (SVM), neural network-based back propagation neural network (BPNN), and tree-based extreme gradient boosting (XGBoost)—were developed to retrieve Cr and Hg concentrations in agricultural soils. The results showed that the fusion of spectral information and environmental covariates combined with the XGBoost model performed best in retrieving both Cr and Hg concentrations in agricultural soils with coefficient of determination (R2) values of 0.73 and 0.74, respectively. Environmental covariates were important variables for determining Cr and Hg concentrations in agricultural soils, but the ability to retrieve these element concentrations by utilizing spectral information alone was limited. High Cr concentrations occurred in central towns and southern hilly mountains. High Hg concentrations were detected in the northwestern region and southern hilly mountains. The potential of fusing spectral information and environmental covariates to precisely retrieve PTE concentrations in agricultural soils can serve as a reference for agricultural soil health information monitoring worldwide.

Nano-micrometer scale characterization of PWSCC crack tips in the transition zone of 52M overlay and the implication to intergranular cracking

This study examines the microstructural characteristics of the primary water stress corrosion cracking (PWSCC) crack tip in the transition zone (TZ) of the 52 M overlay and its implications for intergranular cracking. In the TZ, the Cr content at grain boundaries near the fusion boundary (FB) is lower than those farther from the FB. Additionally, residual strain at grain boundaries near the FB is higher than that farther away, with the fine-grained zone around the FB showing higher local deformation than the surrounding columnar grains. Stress corrosion cracking (SCC) crack growth rate (CGR) test results indicate that the TZ showed certain SCC sensitivity, and the closer to the FB, the lower the SCC resistance. Analysis of the SCC crack tip found that the distinctive composition distribution of the 52 M overlay TZ, characterized by low Cr and high Fe near the FB, is prone to intergranular oxidation, thereby reducing SCC resistance. Conversely, higher Cr and lower Fe content at grain boundaries in the TZ farther from the FB form dense, Cr-rich oxides ahead of the crack tip that slow SCC crack growth, resulting in the diffusion of oxidation along the dislocation structure into the grains and forming a fibrous oxidation zone.

Effect of multi-element synergistic addition on the microstructure evolution and performance enhancement of laser hot-wire cladded Fe-based alloy

To satisfy the requirements of hardness and corrosion resistance for laser additive manufacturing of hydraulic supports, this study applied the synergistic addition of C, B, Cr, Ni, Nb and Mo elements in Fe-based alloys. The multi-phases, martensite + austenite + ferrite were designed. The microstructure, hardness and corrosion resistance of the coatings were analyzed. Increasing the C and B contents could significantly increase the hardness of the coatings, while the corrosion resistance was decreased. The corrosion resistance of the coatings was determined by the Cr contents. However, increasing the Cr contents to 20.0 wt % resulted in the ferrite structure with lower hardness (21 HRC). The coatings with 0.25 wt % C, 1.2 wt % B and 19.0 wt % Cr showed the optimal matching of hardness (56 HRC) and corrosion resistance (survived in neutral salt spray test≥300h). The resulted coatings were mainly consisted of dendritic structure. Fine lath martensite phase was dominant in the dendrite regions. The interdendritic regions were consisted of nano-sized intermetallics with a mixture of σ+Nb + FeNb + Cr2Nb+(Fe,Cr)2B + NbC compounds. These interdendritic regions (14.2 GPa) showed higher hardness than that of the dendritic regions (7.1 GPa). The high Cr contents with finer dendritic structures were the major mechanisms for the excellent combination of hardness and corrosion resistance. The precipitation and growth mechanisms of the interdendritic phases were elaborated. This work provides a valuable reference for laser hot-wire cladding to prepare Fe-based alloys with high hardness and excellent corrosion resistance.

Sustainable Removal of Cr(VI) from Wastewater Using Green Composites of Zero-Valent Iron and Natural Clays

Composites for efficient removal of hexavalent chromium Cr(VI) from industrial wastewater were obtained by deposition of nano-zero-valent iron (nZVI), synthesized by environmentally friendly synthesis using oak leaf extract, on inexpensive, natural, readily available and cheap natural raw materials, sepiolite (SEP) or kaolinite/illite (KUb) clay, as support. nZVI particles were deposited from the FeCl3 solution of different concentrations, with the same volume ratio extract/FeCl3 solution (3:1), and with different masses of SEP or KUb. Physico–chemical characterization (SEM/EDS, FTIR, BET, determination of point of zero charge) of the composites and nZVI was performed. The results of SEM and BET analyses suggested more homogeneous deposition of nZVI onto SEP than onto KUb, which ensures greater availability of the nZVI surface for Cr(VI) anions. Therefore, the higher Cr(VI) removal at all investigated initial pH values (pHi) of the solution (3, 4 and 5) was achieved with the SEP composites. The adsorption results indicated that the elimination of Cr(VI) was achieved via the combined effect of reduction and adsorption. The removal of total chromium at pHi = 3 was approximately the same as that of Cr(VI) removal for the KUb composites, but lower for the SEP composites, indicating lower removal of Cr(III) compared to the reduced Cr(VI). The SEP/nZVI composite with the highest removal efficiency was applied for Cr(VI) removal from real wastewater at pHi = 3 and pHi = 5. The results demonstrated the high Cr(VI) removal capacity, validated the assumption that a good dispersion of nZVI particles is beneficial for Cr(VI) removal and showed that the produced green composites can be efficient materials for the removal of Cr(VI) from wastewater.

Pollution Characteristics and Source Apportionment of Heavy Metals in Topsoil of Counties Along the Shandong Section of the Yellow River

The 25 counties along the Shandong section of the Yellow River are the core areas for promoting the ecological protection and high-quality development of the Yellow River in Shandong Province. Moreover, it is of great significance to study the current situation, sources, and potential risks of heavy metal pollution in the topsoil in this region. In this study, 103 soil samples were collected from the 25 counties along the Shandong section of the Yellow River, and the contents of eight heavy metals （As, Cu, Pb, Cr, Zn, Ni, Cd, and Hg） were determined. The pollution characteristics of heavy metals were analyzed and evaluated using the geological accumulation index and potential ecological risk index. Correlation analysis and the positive matrix factorization （PMF） model were used to analyze the sources of heavy metals. The results showed that the average contents of Cu and Cr were lower than that of the background values of soils, whereas the average contents of As, Pb, Zn, Ni, Cd, and Hg were 1.16, 1.42, 1.05, 1.14, 2.29, and 1.85 times higher than that of the background values, respectively, and the average contents of all eight elements were lower than the screening value of soil pollution risk in agricultural land. In terms of different heavy metal variations, the coefficient of variation （CV） of Cu and Cd was higher than 0.500, indicating high variations, whereas As, Pb, Cr, Zn, Ni, and Hg showed moderate variation. Cd and Hg were slightly polluted, whereas the other six elements were not polluted. Cd and Hg had a moderate potential ecological risk level, whereas the other six elements were at a low level. Correlation analysis and PMF model showed that the sources of heavy metals in the study area were influenced by four factors, i.e., agricultural activities, natural sources, industrial emissions, and atmospheric dust from coal combustion and vehicle exhaust emissions, and the relative contribution rates were 32.4%, 34.9%, 16.5%, and 16.2%, respectively.

Efficient and highly selective photocatalytic reduction of Cr(VI) by an active two-dimensional covalent organic framework

In this paper, a two-dimensional covalent organic framework material (named HDU-27) with thiazole structure and π-π conjugation has been successfully synthesized using the ligands tri acetaldehyde-based methoxyphenyl and benzo [1,2-d:4,5-d]thiazole-2,6-diamine in an ammonia-formaldehyde condensation reaction and applied to the photocatalytic reduction study of chromium (Cr). The photocatalytic experiments showed that HDU-27 had an excellent photocatalytic reduction of Cr(VI) with a high Cr(VI) reduction efficiency of 99.5 ​% at pH ​= ​2 for 60 ​min. In the presence of interfering ions, HDU-27 exhibited excellent selectivity for Cr(VI). Mechanistic experiments and electron spin resonance characterization identified e− and ·O2− radicals as the main active species in Cr(VI) photocatalytic reduction. In addition, the photocatalytic rate of HDU-27 was significantly accelerated in the Cr(VI)/organic pollutant (RhB, MB, MO) mixed system due to the oxidation of the organic matter and the increase in the separation of photogenerated e−−h+. The cycling experiments demonstrated the excellent reduction stability and recyclability of HDU-27 in the photocatalytic reduction of Cr(VI). HDU-27 is an excellent photocatalyst with potential application for removing organic pollutants and heavy metal ions from contaminated wastewater.

The Study of Olivine Inclusions in Diamonds from Liaoning, China and the Evaluation of Related Thermometers

Olivine is the most abundant mineral in mantle peridotite and a typical inclusion in diamonds, providing essential evidence for the characterization of the diamondiferous lithospheric mantle. Three olivine inclusions in diamonds (OlDia) from Liaoning in the North China Craton (NCC) were exposed for in situ measurements, and the compositional data of 62 other OlDia from Liaoning were collected based on previous reports. The enrichment of TiO2 (>0.1 wt.%) with high Cr# (>50; Cr# = 100Cr/(Cr + Al) by atom) was revealed, despite the predominance of depleted TiO2 contents and high Mg# (92.8–93.2; Mg# =100Mg/(Mg + Fe) by atom) for OlDia. Silica fluid accompanying olivine still trapped in the host diamond was recognized using Raman spectroscopy. Three thermometers were applied to the OlDia, based on the data from Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS) and Electron Probe Micro-Analysis (EPMA), and a temperature range (TLA and TEPMA) of 1080–1380 °C was yielded. With respect to the TLA, Al-in-olivine thermometers were preferred, although there was a smaller deviation between TEPMA and TLA when using the Cr-in-olivine thermometer. The results of these thermometers show a high correlation with TEPMA, enabling their application based on EPMA data. Projections onto 39–42 mW/m2 model geotherms underline a diamondiferous base of the lithospheric mantle beneath the NCC. The lithospheric mantle is characterized by refractory and depleted sections, where enrichment metasomatism may have occurred at the lower roots (161–178 km).

Chromium Affects Mitochondrial Function, Leading to Apoptosis and Autophagy in Turtle Primary Hepatocytes.

Hexavalent chromium (Cr(VI)), a pervasive industrial contaminant, is highly toxic to both humans and animals. However, its effects on turtles are largely unexplored. Our study aimed to investigate the toxic effects of Cr(VI) on the Reeves' turtles (Mauremys reevesii) primary hepatocytes. We exposed hepatocytes to two concentrations (25 μM and 50 μM) of Cr(VI) for 24 h. The results showed that compared to controls, Cr(VI)-treated cells showed elevated antioxidant enzyme activity (catalase (CAT) and superoxide dismutase (SOD)) and increased reactive oxygen species (ROS) levels. Adenosine triphosphatae (ATP) levels decreased, indicating mitochondrial dysfunction. Additionally, we found significant changes in mitochondrial dynamics related genes, with downregulation of mitofusin 2 (Mfn2) and silent information regulator 1 (SIRT1) and a decrease in sirtuin 3 (SIRT3) and tumor protein 53 (p53) mRNA levels. Annexin V-FITC fluorescence staining-positive cells increased with higher Cr(VI) concentrations, marked by elevated bcl-2-associated X protein (Bax) and cysteinyl aspartate specific proteinase (Caspase3) mRNA levels and reduced B-cell lymphoma-2 (Bcl2) expression. Autophagy-related genes were also affected, with increased microtubule-associated protein 1 light chain 3 (LC3-I), microtubule-associated protein light chain 3II (LC3-II), unc-51-like autophagy-activating kinase 1 (ULK1), and sequestosome 1 (p62/SQSTM1) mRNA levels and decreased mammalian target of rapamycin (mTOR) and Beclin1 expression. Taken together, Cr(VI) promotes cell apoptosis and autophagy in turtle hepatocytes by inducing oxidative stress and disrupting mitochondrial function. These findings highlight the serious health risks posed by Cr(VI) pollution and emphasize the need for protecting wild turtle populations.

The Process of Steam Oxidation Degradation of High Cr Steel after 125 000 Hours at 568 °C under 16.5 MPa

AbstractThe aim of this work was to analyze the effect of steam oxidation when TP347HFG grade steel was exposed to industrial conditions for 125 000 hrs at 568 °C under 16.5 MPa pressure. The testing material was acquired from one of the coal power plants operating in Poland. Comprehensive investigations were carried out on the outer surface and cross section of the exposed sample using XRD, SEM/EDS and TEM. The analysis revealed the development of a fine grain oxide scale thickness spanning from 20 to 200 µm, consisting Fe2NiO4 (78 %), Cr1.3Fe0.7O3, Fe2O3 (0.8 %) and Fe3Co (0.8 %). Cross-sectional observations showed the formation of grains rich in Nb precipitates type MX carbonitrides surrounded by M23C6 carbides developed as a continuous net at the grain boundaries. The extent of material degradation under the influence of temperature, pressure and exposure time has been meticulously discussed. Graphical Abstract

Fe-based bulk metallic glass with high thermal stability and corrosion resistance

Fe-based metallic glass is prone to crystallization at high temperature due to its thermodynamic instability, resulting in the loss of many excellent properties. In this work, we developed a new Fe-based bulk metallic glass with high Cr and W refractory elements. The results show that the glass transition temperature Tg reaches 880 K. The very high thermal stability can result in the formation of Cr-Cr bonds, W-W bonds, and (Cr,W)-(C,B) bonds with stronger bond energy in Fe-based bulk metallic glass. Moreover, FeCrWCBY bulk metallic glass exhibits good corrosion resistance in 3.5 % NaCl and aqua regia solutions. The self-corrosion current density of FeCrWCBY bulk metallic glass in NaCl solution is only 8.4 × 10–7 A/cm2, much lower than the result of Fe48Cr15Mo14C15B6Y2, known as amorphous steel. The high thermal stability and excellent corrosion resistance are decoded in details from atomic bonding properties and passivation film characteristics.

Cr-induced structural phase transformation in sputter deposited poly-AlN thin film from wurtzite to rocksalt structure and their effect on the optical properties

We report Cr doping-induced structural phase transformation (PT) in sputter-deposited polycrystalline-AlN thin film from wurtzite (w) to rocksalt (r) structure. Rietveld analysis shows that the steady substitution of Al ions by Cr ions in the w-AlN lattice distorts and compresses the wurtzite lattice along the c-axis. The chemical pressure exerted in the w-AlN lattice by the compression from the doped Cr ions causes the PT, similar to the high-pressure-induced PT in AlN. Post the PT, the r-Al1-xCrxN thin film continues to exhibit compressive residual stress, indicating that such sustained stress may also play a role in stabilizing the metastable r-Al1-xCrxN phase. The structural distortion and the PT also affected the optical absorption characteristics of the w-Al1-xCrxN thin films. The w-Al1-xCrxN exhibit a direct inter-band transition and the band gap (Eg) decreases from ∼ 6.06 eV for pure w-AlN to ∼ 4.15 eV for w-Al0.73Cr0.27N. After the PT, the r-Al0.61Cr0.39N thin film, on the other hand, exhibits an indirect inter-band transition with an Eg of ∼ 1.84 eV. In addition to the change in Eg, a prominent defect band appears at ∼ 4 eV at low Cr% and another band appears at ∼ 0.98 eV at higher Cr%.

Kyanite microstructural and microchemical characteristics reveal differences in growth, deformation and chemical modification: A case study from the Paleoproterozoic suture zone of South Harris, NW Scotland

Based on petrological association, cathodoluminescence (CL), trace element signatures and orientation relationships, two generations of kyanite are distinguished in a high temperature, high pressure garnet-biotite-aluminosilicate bearing migmatite of South Harris, NW Scotland. The migmatite shows a garnet and biotite rich domain (Grt-Bt domain) which is cut at a low angle by a dominantly coarse-grained plagioclase-quartz leucosome. In addition, a fine-grained plagioclase-quartz-kyanite domain (Plag-Qtz-Ky domain) is present intercalated with the Grt-Bt domain and subparallel to the plagioclase-quartz domain. Type 1 kyanite is coarse grained and associated with Bt clusters and garnet within the Grt-Bt domain. It grew relatively early, syn- to post-garnet growth, in a suprasolidus environment resulting in crystallographically determined oscillatory CL and trace element zoning. Grains record evidence of progressive deformation in the crystal plastic regime, where deformation is accommodated by dislocation glide, climb and deformation twinning. The dominant activated slip system is (100)<001> with minor component of <100>, while deformation twins show a ∼ 180° rotation around ∼<001> axis and a twin plane near (001). Grains appear to be impervious to deformation induced diffusion with all zoning remaining sharp despite crystal plastic deformation. Grains in direct contact with the Plag-Qtz-Ky domain show late modification of the CL and trace element signature suggesting melt-mediated interface-coupled dissolution-precipitation reaction. This modification resulted in crosscutting lobate high trace element regions and irregular rims with low Cr and V content. These rims show similar CL and trace element characteristics as Type 2 kyanite which are exclusively seen within the Plag-Qtz-Ky domain suggesting that Type 2 grains are cogenetic with Type 1 rims. Type 2 grains are finer grained than Type 1 grains and show near uniform CL and trace element distributions with rare oscillatory zoned and relatively higher Cr & V bright cores. Type 2 show either no or very localized internal deformation features. However, they exhibit a clear shape preferred orientation which coincides with a crystallographic preferred orientation where the longest shape axis is parallel to <001>. We propose that Type 2 kyanite grains underwent melt-present deformation by rigid body rotation in an externally derived melt with different trace element chemistry than the host rock. This melt thus interacted chemically by melt-mediated interface-coupled dissolution-precipitation reactions with the surrounding rocks forming the Type 1 rims.Our study shows detailed analysis of kyanite is an important tool for giving constraints on the deformation, P–T and melting history of high-grade metamorphic rocks and migmatites.

Asessment of blood urea nitrogen to creatinine ratio as a predictor of mortality in ST-elevation myocardial infarction patients undergoing thrombolytic therapy: a cross-sectional study

Objectives: Given the increasing number of ST-elevation myocardial infarction (STEMI) and the related healthcare expenses and medical outcomes, as well as the frequent occurrence of kidney problems in this patient population, the current research aims to explore the effect of blood urea nitrogen to creatinine (BUN/Cr) ratio on the in-hospital mortality (IHM) of STEMI patients undergoing thrombolytic therapy. Methods: This study is a cross-sectional analytical study conducted in 2021 at Shahid Madani Hospital, affiliated with Tabriz University of Medical Science, which investigated the relationship between the BUN/Cr ratio and IHM in patients with STEMI who received thrombolytic treatment between 2017 and 2019. Patients with other causes of ST elevation, those undergoing dialysis, or those with incomplete medical records were excluded. Data were collected from patient medical records. The primary outcome was in-hospital mortality, with secondary outcomes including the occurrence of heart failure and the need for blood transfusion—chi-square tests for categorical and t-tests for continuous variables. A p-value of less than 0.05 was considered statistically significant. Results: A total of 398 patients were diagnosed with STEMI and treated with thrombolytic 330 (82.9%) patients were men. High BUN and Cr had a significant correlation with high mortality rates (P &lt;0.01). However, BUN/Cr didn’t have a substantial relationship with IHM and one-year mortality (P-value = 0.46). The most common in-hospital complication was heart failure (HF), and a higher need for blood transfusion was significantly related to high rates of BUN/Cr (P &lt;0.01). Conclusions: While high BUN and Cr levels were significantly associated with increased mortality rates, the BUN/Cr ratio was not significantly related to IHM. These results suggest that although elevated BUN and creatinine indicate poor prognosis, the BUN/Cr ratio may not be a standalone predictor of in-hospital mortality. Further research is needed to validate these findings and identify other factors affecting patient outcomes.

Influence of the iron-oxide mass fractions of magnetic powdered activated carbon on its hexavalent chromium adsorption performance in water

Magnetic powdered activated carbon (Mag-PAC) is an effective adsorbent to remove hexavalent chromium (Cr(VI)) from water and can be recovered for reuse. However, the tradeoff between the adsorption performance of Cr(VI) and magnetic properties of Mag-PAC remains unclear. Herein, we prepared a series of Mag-PAC adsorbents containing various iron-oxide mass fractions with FeSO4·7H2O as the precursor, using a facile wet-chemical precipitation route and conducted batch experiments to evaluate the Cr(VI) adsorption performance. Results revealed that Mag-PAC was functionalized by magnetic iron oxide comprising crystalline goethite and magnetite structures. Furthermore, its adsorption performance was highly dependent on pH and was most effective at an initial solution pH of 2. Both the sorption rate constant and Cr(VI) adsorption capacity were greatly influenced by magnetization, and they gradually decreased as the iron-oxide mass fraction increased. Among the prepared adsorbents, Mag-PAC-75 (∼32% wt iron) exhibited not only an excellent Cr(VI) adsorption performance (Langmuir adsorption capacity: 75.76 mg/g) but also effective magnetic properties (saturation magnetization: 9.66 emu/g). Coexisting anions had a negligible competitive effect on Cr(VI) removal by Mag-PAC-75 at an initial pH of 2, whereas the presence of tannic acid markedly improved the Cr(VI) elimination. The presence of trivalent chromium on the surface of Mag-PAC-75 confirmed via X-ray photoelectron spectroscopy indicated that some synergistic redox reactions may occur during the sorption process. After five regeneration cycles using NaOH, Mag-PAC-75 continued to exhibit a high Cr(VI) removal efficiency and magnetic stability. These findings indicate that optimizing the adsorption performance and magnetic properties is a key factor for realizing the practical application of Mag-PAC for Cr(VI) removal. Overall, Mag-PAC may have been a promising application prospect for Cr(VI) removal from water due to its high adsorption capacity and magnetic properties, coupled with its good reusability and magnetic stability after regeneration cycles.

Rational synthesis of highly efficient dual–Z–scheme InVO4/FeVO4/Ex–CQDs–g–C3N4 heterojunction for photo(electro)chemical water splitting and pollutant removal applications

BackgroundThe ever–growing concern for environmental pollution and the need for clean energy sources have driven research toward sustainable technologies. Semiconductor photocatalysis has emerged as a promising approach for both environmental remediation and clean energy generation due to its efficiency and environment–friendly nature. This work focuses on developing a novel photocatalyst capable of addressing two crucial environmental challenges: Cr(VI) removal and water splitting for clean hydrogen production. MethodsThis study presents the development of a dual–Z–scheme heterojunction photo(electro)catalyst based on a combination of metal vanadates (FeVO4 and InVO4) and ultrasound–exfoliated carbon–rich graphitic carbon nitride (Ex–C–g–CN), denoted as IVO/FVO/Ex–C–g–CN. The synthesized nanocomposite was thoroughly characterized using various spectroscopic and microscopic techniques (such as XRD, XPS, UV–DRS, FESEM, EDX, and PL) to understand its material properties and structure. These techniques are crucial for elucidating the relationship between the composition of the material and its photocatalytic performance. Significant findingsThe key innovation of this work lies in the design of the dual–Z–scheme heterojunction within the IVO/FVO/Ex–C–g–CN photo(electro)catalyst. This design fosters efficient separation of photogenerated charges, a critical factor for enhancing photocatalytic activity. The effectiveness of this approach is evident in the achieved removal efficiency of 97.17 % for 100 ppm Cr(VI) within just 60 min of visible light irradiation. This demonstrates the superior ability of the developed photocatalyst to address chromium contamination. Furthermore, the photocatalyst exhibits a remarkable photocurrent of 3.16 mA and a low onset potential of 112 mV for the photoelectrochemical oxygen evolution (OER) reaction. These findings highlight the potential of this material for solar–driven water splitting, a clean and sustainable method for hydrogen production. Additionally, the IVO/FVO/Ex–C–g–CN composite demonstrates excellent recyclability, maintaining high Cr(VI) removal efficiency over multiple cycles, indicating its reusability and cost-effectiveness. Overall, the exceptional photo(electro)catalytic performance of the IVO/FVO/Ex–C–g–CN dual–Z–scheme heterojunction positions it as a promising candidate for tackling environmental pollution and generating clean energy.

Effect of in situ CO2 mixing of cement paste on the leachability of hexavalent chromium (Cr(VI))

In situ CO2 mixing technology is a potential technology for permanently sequestering CO2 during concrete manufacturing processes. Although it has been approved as a promising carbon capture and utilisation (CCU) method, its effect on the leachability of heavy metals from cementitious compounds has not yet been studied. This study focuses on the effect of in situ CO2 mixing of cement paste on the leaching of hexavalent chromium (Cr(VI)). The tank leaching test of the CO2 mixing cement specimen resulted in a Cr(VI) cumulative leaching of 0.614 mg/m2 in 28 d, which is ten times lower than that of the control mixing specimens. The results in thermogravimetric analysis indicated that a relatively significant amount of CrO42− is immobilised as CaCrO4 during the CO2-mixing, and a higher Cr–O extension is observed in the Fourier transform infrared spectra. Furthermore, a portion of the monocarboaluminate is inferred from microstructural analyses to incorporate CrO42− ions. These results demonstrate that in situ CO2 mixing is beneficial not only in reducing CO2 emissions, but also in controlling the leaching of toxic substances.

Precisely constructed core-shell organic/inorganic heterojunction for heightened photoreduction of Cr(VI): Synergy of reinforced interface interaction and high-speed carrier transfer

Photocatalysis technology has been widely studied for treating Cr(VI) pollution in water and constructing heterogeneous structures presents a compelling approach to enhance the efficiency of Cr(VI) treatment. Pitifully, solely utilizing heterostructure, especially random composites of heterogeneous photocatalysts, often falls short of effectively enhancing the separation efficiency of photogenerated carriers. Furthermore, most photocatalysts interact weakly with the Cr(VI) anions, greatly reducing the utilization efficiency of photogenerated carriers. Herein, pyridine-based conjugated imprinted polymer (CIP) photocatalyst was precisely coated on urchin-like TiO2 using an in-situ condensation approach, forming a compact core–shell structure of organic/inorganic heterojunction. On the one hand, the compact heterojunction structure of the core–shell effectively improved the separation efficiency of photogenerated carriers. On the other hand, CIP enhanced the adsorption between the photocatalyst and Cr(VI), effectively improving the utilization efficiency of photogenerated carriers. Due to the collaborative effects of selective adsorption and core–shell heterojunction photocatalysis, the photocatalyst demonstrated remarkable performance in eliminating Cr(VI). For high concentration Cr(VI) pollution of 100 ppm, complete elimination could be achieved within 90 min. This research presented an innovative and efficient approach for the precise synthesis of photocatalysts.

Accelerated High-Temperature Oxidation Behavior of Ferritic Stainless Steel under Air/H2+H2O Dual Atmosphere

Improvement in durability is one of the important subjects for utilizing solid oxide electrolyzer cell (SOEC) systems widely. In SOEC stacks, separators are exposed to complexed dual atmosphere (i.e. hydrogen - steam mixed gases and oxygen rich air are on each side). In this study, the degradation phenomena of separator materials (SUS430, ZMG232G10, Crofer22APU) in SOEC dual atmosphere were investigated. The samples were exposed in SOEC dual and simple atmospheres at 700 °C for 500 h. Then, their cross sections were analyzed by X-ray diffraction and scanning electron microscopy/energy-dispersive X-ray analysis. The degradation mechanisms of the separator materials in the SOEC stack operating conditions were discussed. ZMG232G10 and Crofer22APU with high Cr content showed thin oxide layer under both the dual or single atmosphere, while SUS430 with low Cr content showed significant oxidation in the H2-steam atmosphere and on the air side under the dual atmosphere condition. The significant oxidation on the air side of the dual atmosphere of SUS430 observed in this study is a unique phenomenon under the dual atmosphere condition and not observed in a single air atmosphere.