High Cr Research Articles

Highly efficient reduction of Cr(VI) from industries sewage using novel biomass-driven carbon dots modified TiO2 under sunlight

Hexavalent chromium (Cr(VI)) pollution poses a significant global environmental challenge, with current photocatalysts exhibiting limited efficiencies under natural sunlight, especially in neutral to alkaline conditions or at high Cr(VI) concentrations. In this study, amine-rich biomass-derived carbon dots (CDs) were synthesized from peanut shells and ethylenediamine via a hydrothermal method, combined with titanium dioxide (TiO2) to form a composite with a narrower band gap. This enhanced the electrostatic interactions with Cr(VI), thus improving photocatalytic performance. The composite (1 % CDs) effectively reduced 50 mg/L of Cr(VI) within 60 min under sunlight irradiation, demonstrating stable performance across various pH levels (3, 5, 7, and 9) and Cr(VI) concentrations (10 to 60 mg/L). Even after five cycles, the reduction efficiency remained high at 96.83 %. The composite also achieved reduction rates of 90.09 % and 89.01 % for domestic and electroplating wastewater, respectively, while exhibiting antibacterial properties. Free-radical scavenging experiments confirmed that electrons and holes were the primary active species driving the reduction. This work highlights the potential of the composites for efficient and stable Cr(VI) reduction in real-world water treatment applications.

Molecular dynamics simulation of friction in DLC films with different Cr doping levels

This study systematically investigates the impact of varying Cr doping levels on the friction properties of DLC films using molecular dynamics simulations. The results demonstrate that under identical friction velocities and load conditions, the friction force of DLC films significantly decreases when the Cr doping content reaches 16.5 %. High Cr doping levels lead to the formation of Cr atomic clusters at the interface, hindering contact and reducing the number of interface bonds. These clusters act as lubricants, filling the interface gaps and thereby reducing the friction force. Internal stress calculations indicate that Cr doping effectively reduces the average internal stress of DLC films. For DLC films with lower Cr doping levels, the friction force exhibits similar trends under different friction velocities, while films with higher Cr doping levels show a more pronounced response, with friction force increasing at higher velocities. Increasing the load significantly raises the friction force, especially for DLC films with higher Cr doping levels. Furthermore, high Cr doping levels under high loads lead to significant structural damage and adhesive wear. This study provides theoretical and technical references for optimizing the friction performance of DLC films.

Assessing Metals and Metalloids Impact of Roadside Dust on Human Health in Osogbo, Osun State, Nigeria

BackgroundMetals and metalloids in roadside dust pose considerable threats to both human health and the environment. ObjectivesThis study assesses human health risks of metal exposure to roadside dust by conducting a health risk assessment (HRA) for metals and metalloids uptake rates for children and adults via exposure pathways. MethodsSettled dust samples were collected from the major roads in Osogbo, Osun state. These samples were subjected to standard laboratory procedures for metals and metalloids analysis using Atomic Absorption Spectroscopy (AAS). ResultsAll the metals and metalloids except Cd had their concentration below the WHO limit. The average concentration of Cd was 1.54 mg kg-1, significantly above the WHO guideline of 0.80 mg kg-1, indicating a possible health concern. A strong positive correlation exits between Ni and Cd (.774⁎⁎) (p<0.01), Pb (.662⁎⁎) (p<0.01), Zn (.606⁎⁎) (p<0.01), and As (.549*) (p<0.05), showing that greater Ni concentrations are associated with higher concentrations of Cd, Pb, Zn, and As. Two principal components were identified, accounting for 80% of the overall variation. PC1 has an eigenvalue of 60.834; however, PC2 has a higher eigenvalue of 74.952, implying that PC2 explains more of the variation in the data than PC1. Non-carcinogenic risk evaluations identify possible health risks linked with Cu, Cd, Cr, and As exposure, primarily through inhalation routes. Carcinogenic risk showed that Cd demonstrated high CR values ranging from 3740 to 1.30*1012 for adults and children throughout the study's various exposure paths. ConclusionThis study offered significant insight into the metals and metalloids pollution status in Osogbo, Nigeria, employing data and statistics, highlighting the need for evidence-based actions for environmental preservation to safeguarding people's health.

Origin of the Oligocene–Miocene Sailipu ultrapotassic volcanic rocks in southern Tibet: Melting of Asian mantle pyroxenites triggered by eastward tearing of the subducting Indian continental slab

Widely distributed Oligocene−Miocene ultrapotassic volcanic rocks in the Lhasa terrane of southern Tibet have been associated with the melting of the lithospheric mantle, plateau uplift, and porphyry Cu-Au mineralization. This study presents the mineral chemistry of olivine and clinopyroxene phenocrysts, whole-rock major and trace element data, and zircon U-Pb geochronological and Hf isotopic data for the Sailipu primitive ultrapotassic volcanic rocks. The Sailipu volcanic rocks exhibit high MgO (5.6−11.4 wt%), Cr (386−981 ppm), Co (22−43 ppm), and Ni (95−423 ppm) concentrations and have highly fractionated rare earth elements [REEs; (La/Yb)N = 23−73] and high-Fo (89.1−90.8) olivine phenocrysts containing elevated NiO (up to 0.59 wt%), which suggests a pyroxenitic mantle source that partially melted in the garnet stability field. Their high K2O contents (4.8−8.0 wt%) and global subduction sediment-like trace element patterns suggest that the metasomatic agents, which reacted with mantle peridotites to form phlogopite-bearing pyroxenites, were dominantly derived from the melting of subducted continental sediments. Their high whole-rock Ba/La and Th/Nd ratios are consistent with this hypothesis. The Sailipu ultrapotassic volcanic rocks also exhibit low initial 176Hf/177Hf ratios that resemble those of Himalayan leucogranites, and high Ca contents in olivine phenocrysts, which is consistent with contributions from the subducted carbonate-rich sedimentary strata on top of the thinned Greater Indian continental crust. The zircon U-Pb chronological data yielded concordant ages of 24.33 ± 0.19 Ma, 21.20 ± 0.62 Ma, and 17.05 ± 0.31 Ma for different exposures of the Sailipu volcanic rocks, which establishes a maximum age of ca. 24 Ma for these rocks. The northwest−southeast spatial distribution and the southeastward decrease in age (80°E−90°E) suggest west-to-east tearing of the thinned Greater Indian slab, which caused asthenospheric upwelling and melting of the Tibetan lithospheric mantle. Geothermometric calculations show relatively high primary magma temperatures (∼1250 °C) that are consistent with asthenospheric upwelling. We propose a mechanism that could genetically link the coeval Cu-Au ore-forming granitoids with the ultrapotassic magmatism of the Gangdese belt. The ultrapotassic rocks supply a large-volume of external magmatic volatiles, particularly H2O, which could trigger melting of the Tibetan lower crust and lead to the generation of the ore-forming granitoids and the establishment of oxidizing conditions for porphyry deposits. The oxygen fugacity (log ƒO2 values of ΔFMQ) of the primitive Sailipu ultrapotassic volcanic rocks (ΔFMQ = 0.48 ± 0.51 based on the Dol/melt V oxybarometer and ΔFMQ = 0.33 ± 1.19 according to the magmatic zircon U-Ce-Ti oxybarometer) is slightly lower than that of porphyry Cu-Au ore-forming granitoids in the eastern Gangdese (ΔFMQ = +0.8 to +2.9), which suggests that the direct injection of ultrapotassic melts into ore-forming granitoids played a limited role in changing oxygen fugacity, but more oxidized fluids/volatiles exsolved from these ultrapotassic melts may have facilitated the remelting of sulfide-bearing lower crust and/or directly scavenged sulfides from the mush-state reservoirs of the ore-forming granitoids in the middle−upper crust.

Investigation of softening in hardfaced layers during welding

Hardfacing is a widely used technique to create wear-resistant layer on the base material to ensure good durability and performance under harsh operating conditions. However, despite its effectiveness in improving wear resistance, hardfaced layers can sometimes exhibit softening phenomena during welding, compromising their mechanical properties and overall performance. In this research, the effect of heat input was investigated in case of Fe-based hardfacing material with high Cr content. 4 different heat inputs were applied with gas metal arc welding and significant differences were determined in hardnesses, which can be influential to the lifetime of hardfaced parts. Hardness drop happens in the heat-affected zones between the hardfaced layers and the highest heat input causing the most significant softening (20% hardness drop).

Unraveling the Subsurface Damage and Material Removal Mechanism of Multi-Principal-Element Alloy FeCrNi Coatings During the Scratching Process

Multi-principal-element alloys (MPEAs) exhibit superior strength and good ductility. However, tribological properties of FeCrNi MPEAs remain unknown at nanoscale and complex environments. Here, we investigate the effects of scratching speed, depth, and temperature on microstructural and tribological characteristics of FeCrNi using molecular dynamics simulations combined with an elevated temperature tribological experiment. The scratching force experiences the increase stage, the undulated stage, and the stable stage due to chip formation. Compared to traditional alloy coatings, low force enhances the useful life. With increased speed, the friction coefficient decreases, agreeing with previous work. High speed impacting includes severe local plastic deformation, from dislocation to amorphization. As the scratching depth increases, the average scratch force and friction coefficient increases owing to material accumulation in front of the abrasive particles. The surface morphology and dislocation behavior are significantly different during the scratching process. In addition, we revealed a temperature-dependent friction mechanism. FeCrNi MPEAs have excellent wear resistance at an intermediate temperature, which is attributed to the high Cr content promoting the formation of the compact oxide layer. This work provides atomic-scale mechanistic insights into the tribological behavior of FeCrNi, and would be applied to the design of MPEAs with high performance.

Origin and metamorphism of ophiolitic serpentinites from the Yuli belt, eastern Taiwan: new findings and tectonic implications

ABSTRACT Serpentinites associated with metamafic and metaplagiogranitic rocks occur sporadically within metasedimentary schists in the Yuli belt. Such metaigneous rocks are considered to represent ophiolitic protoliths and some contain high-pressure (HP) metamorphic minerals or assemblages. However, the origin and metamorphism of these serpentinites have long been a mystery. This study systematically investigates the four major serpentinite-bearing exposures at the Fengtien, Wanjung, Tsunkuanshan, and Chinshuichi. The results reveal that the serpentinites are of two different protoliths on the basis of relict chromian spinel composition. Cr-spinel compositions of the Fengtien and Tsunkuanshan samples are characterised by moderate Cr# [Cr/(Cr + Al)] (0.45–0.57), relatively high Mg# [Mg/(Mg+Fe2+)] (0.59–0.79), but low Fe3+# [Fe3+/(Fe3++Cr+Al)] (0.02–0.06), reflecting an abyssal peridotite type protolith. By contrast, Cr-spinel compositions of the Wanjung and Chinshuichi samples show high Cr# (up to 0.74) and Fe3+# (0.03–0.08), but low Mg# (<0.6), indicating a forearc mantle peridotite origin. Peak metamorphic conditions of the serpentinites are represented by the assemblage of antigorite + magnetite + chlorite + olivine + diopside, which is estimated as up to 550°C but the pressure cannot be constrained quantitatively. Based on field relations, it is inferred that the serpentinites, associated HP metaigneous rocks, and garnet-bearing metasedimentary schists were metamorphosed isofacially. Despite two origins, the peridotitic protoliths were all subjected to hydration and subduction processes. We suggest that precursors of the serpentinites, metaigneous rocks, and metasedimentary schists were juxtaposed and metamorphosed at intermediate to great depths (~35–55 km) of a subduction zone. Therefore, the Yuli belt serpentinites and associated rocks likely represent exhumed materials from a palaeo-subduction interface.

On the formation of oxide inclusions in the high nitrogen chromium-manganese steel produced by the Wire and Arc Additive Manufacturing

Oxide inclusions significantly impeded the mechanical properties of the Wire and Arc Additive Manufacturing (WAAM) made high nitrogen Cr–Mn austenite stainless steels (HNSs). This paper focused on the inclusions' component, crystallization characteristics and formation mechanism. Results revealed that there are two types of inclusions: the round-shape nano-size inclusion (Type-I) and the micron-size island-shape inclusion (Type-II). The Type-I inclusion usually consists of the MnO particle or the combination of the MnO, Si-oxides and precipitations (MnS or Cr2N). Most of the Type-I oxide inclusion is located in the range between 300 nm and 700 nm,the number of Type-I oxide inclusion takes the main part of 69.7%.With higher content, smaller size and more even distributions, the isolated Type-I oxide inclusions would be beneficial to the mechanical properties owing to the Orowan strengthening mechanism. The Type-II inclusion is mostly composed of the MnO matrix and the coherent chromite spinel (MnCr2O4). In general, the larger the size, the more serious the negative impact on mechanical properties. And there was a strong negative correlation between the size and quantity of type II oxide inclusions. After heat treatment, abundant phase transformations occurred in the Type-II inclusions and some harmful phases (Sigma, MnS et cl.) were often found in or around the inclusions with specific orientation relationships. During deposition, the unstable droplet transformation and the trapped residual slag were the main causes for the inclusions in the molten pool.

Risk factors for postoperative hepatic dysfunction in overweight patients with acute type A aortic dissection

BackgroundAcute hepatic dysfunction (AHD) is a common postoperative complication in patients with acute type A aortic dissection. The aim of this study was to identify risk factors for acute hepatic dysfunction after surgery for acute type A aortic dissection.MethodsWe performed a retrospective study from March 1, 2019, to February 28, 2021. The primary endpoints of this study were morbidity due to AHD and risk factors for incidence. Univariate analysis and multivariate logistic regression analysis were used to analyse the related factors, and receiver operating characteristic (ROC) curves were plotted to evaluate their predictive value.ResultsAmong 147 patients, 29 (19.73%) developed postoperative acute hepatic dysfunction, and 9 (6.12%) died. Univariate analysis revealed that the ALT (P = 0.042), Cr (P < 0.001), and BUN (P = 0.008) levels were significantly different between the two groups. Multivariate logistic regression analysis revealed that Cr (OR = 1.013, 95% CI = 1.003–1.023, P = 0.008) was an independent risk factor for postoperative hepatic dysfunction in overweight (BMI > 24) patients with ATAAD. The area under the ROC curve (AUC) for Cr was 0.745 > 0.7, indicating good predictive value.ConclusionA high Cr concentration is an independent risk factor for postoperative AHD in overweight (BMI > 24) patients with ATAAD.

Effect of Cr:C ratio on open three-body wear resistance of squeeze cast high chromium cast iron

A series of high chromium white cast iron (HCCI) alloys with varying Cr:C ratios were designed and fabricated through the squeeze casting process. This study investigates the effect of the Cr:C ratio on the mechanical properties, microstructure, phase diagram, and both low-stress and high-stress abrasion performance of HCCIs. Alloys with a very high Cr:C ratio exhibited better impact toughness but poorer hardness. Scanning electron microscopy (SEM) and phase diagram calculations elucidated the influence of the Cr:C ratio on microstructure, carbide volume fraction, and carbide type. Abrasion resistance was evaluated using impact abrasive wear (high-stress) and rubber-wheel (low-stress) abrasion on quartzite in open three-body wear. Comprehensive assessments under impact abrasive wear and rubber-wheel abrasive wear conditions suggest that the alloy achieves optimal abrasion resistance with a Cr:C ratio ranging from 8 to 11. Post-wear analysis reveals that surface damage varies between high-stress and low-stress conditions. The microstructure of squeeze HCCIs is significantly influenced by the Cr:C ratio, resulting in diverse operative wear mechanisms, including micro-cutting and micro-fracture. Successful adjustment of the Cr:C ratio led to the attainment of a nearly eutectic HCCIs composition suitable for squeeze casting.

Optimizing propylene production via acetone hydrodeoxygenation: Insights from catalytic studies with Cu/γ-Al2O3 and Hβ zeolite

Propylene is a crucial light olefin in the petrochemical industry and can be produced via acetone hydrodeoxygenation, which involves two sequential reactions: first, acetone undergoes hydrogenation catalyzed by metallic sites, followed by the dehydration of the resulting isopropanol catalyzed by acidic sites. In this study, propylene production through acetone hydrodeoxygenation was investigated using a physical mixture of 35 wt% Cu/γ-Al2O3 and Hβ zeolite to investigate how various reaction parameters affect acetone conversion and propylene yield. Using the experimental design methodology, empirical models were developed to correlate acetone conversion (Xacet) and propylene yield (Yprop) with the ratio of 35 wt% Cu/γ-Al2O3 to Hβ (CR), total catalyst weight (Cw), hydrogen volumetric flow rate (FH2) and reaction temperature (T). The maximum propylene yield achieved in the catalytic tests was 73.46 %. A long-term test demonstrated the catalyst's reusability, remaining active even after 22 hours of reaction with only a slight decrease in propylene yield. Analysis of the experimental data revealed that increasing T and Cw positively affected propylene yield, whereas higher CR and FH2 had negative effects. According to the Pareto chart, reaction temperature was the most influential variable for propylene yield, followed by CR, FH2 and Cw. For acetone conversion, the order of significance among the variables was T >CR >Cw >FH2.

Recovering chromium from electroplating sludge using an integrated technology of bipolar membrane electrodialysis and H2O2 oxidation

Chromium electroplating produces Cr(III)-containing electroplating sludge (EPS) in large volumes, which is easily oxidised to Cr(Ⅵ) and is harmful to the environment and human health. This study recovered Cr(III) as Na2CrO4 from EPS using an integrated bipolar membrane electrodialysis (BMED)–H2O2 oxidation technology. During the treatment process, Cr(III) was oxidised to Cr(VI) using H2O2 in an alkaline environment, BMED was used to separate and recover Cr(VI). Experimental results showed that H2O2 dosage and pH affected Cr(III) oxidation—the highest Cr(III) oxidation ratio of 68.4% was observed when H2O2 dosage and pH were 5.5 mL and 12.0, respectively. The current density, solid/liquid ratio and sludge particle size affected Cr(III) recovery, energy consumption and current efficiency. Under a current density of 20.0 mA/cm2, solid/liquid ratio of 1.0:45 and sludge particle size of 100 mesh, 58.2% of Cr(III) was recovered. When the number of the equipped EPS compartments was increased from one to two and three, the specific energy consumption decreased from 1.04 to 0.87 and 0.81 kW h/g, respectively, but the current efficiency remained almost constant. After EPS treatment, the Cr(III) remaining in the sludge was mainly in the residual state, which is less environmentally harmful. The obtained Na2CrO4 had similar properties according to X-ray diffraction analysis. Thus, the proposed integrated technology effectively recovers Cr(III) from EPS and other chromium-containing solid wastes.

Feasibility and mechanism of adsorption and bioreduction of hexavalent chromium using Rhodopseudomonas palustris immobilized on multiple materials

Rhodopseudomonas palustris immobilized on multiple materials was used to invistigate Cr(VI) adsorption and bioreduction. The highest Cr(VI) removal (97.5%) was achieved at 276h under the opitimed conditions of 2.5% SA, 8% PVA, and 50% filling degree. The highest adsorption capacity was obtained at 11.75 mg g−1 under 300 mg L−1 Cr(VI). Results from adsorption kinetics and isotherms indicated that Cr(VI) adsorption of immobilized photosynthetic bacteria (IPSB) was consistent with the Freundich model and the pseudo-second-order kinetic model (qe = 14.00 mg g−1). SEM and FTIR analyses verified that the porous multilayer network structure of IPSB provided more adsorption sites and functional groups for the removal of Cr(VI). Furthermore, the maximum Cr(VI) reduction efficiency of IPSB was achieved at 10.80 mg g−1, which correlated with the up-regulation of chrR gene expressions at 100 mg L−1 Cr(VI). This study demonstrated the dual mechanisms of Cr(VI) removal in IPSB-treated Cr wastewater, involving both chemisorption and bioreduction working synergistically.

Mechanistic insight into the simultaneous removal of Cr(VI) and phosphate by a novel versatile bimetallic material

Industrial wastewater containing hexavalent chromium Cr(VI) and phosphate poses a great threat to human health and the aquatic ecological environment. In this study, a novel La(OH)3- and CaO2-fabricated CNT (La-Ca-CNT) material was developed for the simultaneous and highly effective removal of aqueous Cr(VI) and phosphate. Characterization results showed that synergistic effects existed between the CNT support and La and Ca species. La-Ca-CNT showed high phosphate and Cr(VI) removal rates in acidic conditions with high stability. Kinetic study suggested that the fast adsorption of phosphate on La-Ca-CNT was controlled by intraparticle diffusion. The removal of Cr(VI) and phosphate interacted with each other, and the removal of Cr(VI) went through a slow-fast-slow reaction, reaching a Cr(VI) removal rate of over 97% within 180min. La-Ca-CNT had a high phosphate adsorption capacity (174.3mg/g), and over 70% of the adsorbed phosphate could be recovered. The presence of co-existing anions showed negative effects on phosphate adsorption but negligible effects on Cr(VI) reduction, while organic carbon in natural water showed no effect on phosphate and Cr(VI) removal. A mechanistic study revealed that phosphate was removed by physical-chemical adsorption (outer-sphere complexation and ligand exchange) over La-Ca-CNT, while Cr(VI) was reduced by H2O2 generated from CaO2 or directly by surface CaO2.

A study on microstructure evolution of MCrAlY coatings after thermal aging in Te environment

The effects of thermal exposure on tellurium (Te) diffusion behavior in MCrAlY coatings were investigated at 800 °C in Te vapor. The results showed that the diffusion depth of Te in MCrAlY coatings gradually increased with the exposure time, and the dense Cr3Te4 layer formed on the coating surface in the initial stage was no longer continuous, especially under aging conditions with higher Te concentration. The high Cr content of the coating promoted the solid phase transition of the surface reaction product from Cr3Te4 to Cr7Te8, and resulting in the formation of large α-Cr phase either within or beneath the reaction layer during long aging processes. As a result of this phase transition, excess Te atoms were released from Cr3Te4 and continued to diffuse into the coating. Te did not exhibit obvious intergranular diffusion characteristics within the coating. When it encountered Y, it was captured by Y and formed a YTe phase. After aging for 3000 h, Te was distributed throughout the coating, and numerous voids were formed at the interface between the coating and the substrate. These two factors deteriorated the plasticity and adhesion of the coating. Results from molten salt corrosion tests indicated that the high content of Cr and Al in the coating, as well as high densities of grain boundaries providing diffusion pathways, reduced the corrosion resistance of the coating to molten salt.

Unraveling the Protolith Origin of Serpentinite Rocks from the Tengnoupal Area, Manipur Ophiolite Complex, Indo-Myanmar Range

Objective: This article mainly focuses on investigating the protolith origin of serpentinite rocks in and around Tengnoupal, within the Manipur Ophiolite Complex (MOC), using a combined petrographic and geochemical approach. Methods: During fieldwork, samples were collected and cut into thin sections to reveal their mineralogical and textural relationships. Major oxides and trace elements were determined by XRF, and rare earth elements analysis was carried out by ICP-MS to determine the nature and origin of the rocks. Findings: The studied rock samples exhibit varying degrees of serpentinization, ranging from partial to complete, and exhibit a pseudomorphic texture including mesh and hour structures replacing the original olivine and bastite texture replacing pyroxene. Geochemically, the analyzed rock types exhibit komatiitic affinity and are characterized by high magnesium numbers (Mg# average 84.4). The studied serpentinite rocks have lower Al/Si ratios (Average=0.05) and higher Mg/Si ratios (average= 0.95) in bulk rock compositions indicating a refractory abyssal mantle peridotite protolith when compared to the primitive mantle. The high Ti (range 300-480 ppm) and Cr (628-3186 ppm) contents indicate a subduction environment. In addition, the rock samples exhibit slight depletion chondrite-normalized Rare Earth Elements (REE) patterns ((La/Yb) N = average 0.87). The rocks exhibit spoon-shaped normalized Rare Earth Element patterns and primitive mantle are similar to mid-oceanic ridge abyssal mantle rocks. Novelty: The origins of the rocks studied suggest a transitional phase between abyssal and subduction zone-related serpentinites, forming after harzburgite-peridotite. As subduction began, dehydrated orogenic peridotite from the abyssal serpentinites was thrust or obducted, forming the MOC serpentinites. This indicates that the serpentinite rocks in MOC share similarities with those found in mid-oceanic ridge environments, which is characteristic of a supra-subduction zone setting. Keywords: Ultramafic rocks, Serpentinization, Supra­subduction zone, Abyssal, REE

Influence of Heat Treatment on Erosive Wear Resistance of High Cr Cast Irons

Influence of Heat Treatment on Erosive Wear Resistance of High Cr Cast Irons

Steam Stripping for Recovery of Ammonia from Wastewater Using a High-Gravity Rotating Packed Bed

Steam stripping of ammonia from ammonia-rich wastewater (5000–20,000 mg/L) was conducted in a continuous-flow rotating packed bed (RPB) at a pH of 11. This study aimed to elucidate the influence of key operational parameters, including the steam-to-liquid ratio, rotational speed (ω), initial ammonia concentration, steam inlet temperature (TSi), and liquid inlet temperature (TLi), on critical performance metrics such as the ammonia removal efficiency (ARE), the volumetric liquid mass transfer coefficient (KLa), and the concentration of the recovered ammonia solution (CR). The findings revealed that a CR of 22.88 wt.% was achieved under the optimal conditions of a steam-to-liquid ratio of 0.175 kg/kg, an initial concentration of 20,000 mg/L, a TSi of 120 °C, and a TLi of 70 °C. Key experimental factors, including the initial ammonia concentration, TSi, and TLi, significantly impacted the achievement of higher ARE and CR values. The KLa values exhibited a decrease with the increase in the steam-to-liquid ratio, while they increased with ω. However, the KLa remained relatively consistent with ω values within the range of 600 to 1200 rpm. In comparison with prior studies, steam stripping of ammonia exhibits a higher ARE than air stripping with RPB and a higher CR than conventional stripping methods. Moreover, RPB requires a smaller size to achieve equivalent ARE compared to conventional stripping apparatuses. Thus, the steam stripping process with RPB equipment emerges as a suitable method for ammonia recovery from ammonia-rich wastewater.

Geochemistry and conditions of formation of Mesoarchean banded iron formations (BIF-1) from the Kostomuksha Greenstone belt, Karelian Craton

Three variably old groups of banded iron formation (BIF) are known in the Kostomuksha Greenstone belt (KGB) of the Karelian Craton. This paper deals with the earliest of them, Mesoarchean (2.87–2.81 Ga) – BIF-1. BIF-1 occurs among the komatiite-basalt unit of the KGB. BIF-1 consists mainly of quartz and magnetite, with varying amounts of amphibole, biotite, and garnet; they contain 48.3-58.6 SiO2 and 21.34–33.82 wt. %, Fe2O3T, suggesting that the rocks are BIF. BIF-1 of the KGB, as well as most Archean BIFs, contain high Fe2O3T, concentration, display a contrasting positive Eu anomaly, lost of Ce anomaly, the depletion of LREE relative to HREE. However, they stand out among other BIFs with high Al2O3, TiO2, MgO, K2O, Cr, Ni, Zr, Ba, Cu and Zn concentrations. BIF-1 was formed in a marine basin in an anoxic atmosphere due to hydrothermal fluids, the proportion of which varies from 20 to 80 %, and a terrigenous component derived mainly from basalts, komatiites, and dacites in host rocks. Mesoarchean BIF-1 of the KGB s was formed in a small rift within an oceanic volcanic plateau, the formation of which is associated with the influence of a mantle plume on the oceanic lithosphere.

Thermal corrosion behavior of Inconel 693, Hastelloy N and 310S in ceramic waste forming reactions

The thermal corrosion behavior of Inconel 693, Hastelloy N, and 310S was investigated in the reaction environment of ceramic waste forming reactions. Due to the difference in Cr content and the effect of chlorides, the high Cr Inconel 693 and 310S alloys exhibit selective corrosion by Cr, while the low Cr Hastelloy N exhibits uniform corrosion and the volatilization of MoO3 caused high dimensional losses. The different behavior of the alloys in different corrosive environmental regions is also discussed. In the sintered product region, due to the encapsulation of the sintered product and the corrosion inhibiting role played by O2−, Hastelloy N alloy and 310S alloy experienced milder corrosion compared to alloy in the atmosphere region. And in the atmosphere region, the more abundant gas supply and the open environment caused Hastelloy N alloy and 310S alloy to experience more severe erosion. However, for Inconel 693 alloy, it formed a continuous spinel phase layer containing FeCr2O4 due to the higher partial pressure of O2 in the atmosphere region, resulting in more slight corrosion compared to the sintered product region.