Fe Addition Research Articles

Suppression of discontinuous precipitation by Fe addition in Cu–Ti alloys

Suppression of discontinuous precipitation by Fe addition in Cu–Ti alloys

Distinct responses of diatom- and flagellate-dominated Antarctic phytoplankton communities to altered iron and light supply

Primary production in the Southern Ocean is strongly influenced by the availability of light and iron (Fe). To examine the response of two distinct natural Antarctic phytoplankton communities (diatom vs. flagellates) to increasing light and Fe availability, we conducted two shipboard incubation experiments during late summer and exposed each community to increasing light intensities (30, 80, and 150 µmol photons m−2 s−1) with or without Fe amendment. Our results show clearly that both communities were Fe-limited since Fe addition resulted in higher particulate organic carbon (POC) production rates. The magnitude of the Fe-dependent increase in POC production, however, varied between the two stations being higher in the diatom-dominated community relative to the flagellate-dominated community. This differential response to increasing Fe supply could be attributed to the higher Fe requirement of the flagellate-dominated assemblage relative to the diatom-dominated assemblage. Irrespective of Fe availability, light also strongly stimulated the POC production of both communities between low and medium light supply (30 versus 80 µmol photons m−2 s−1), indicating that both assemblages were light-limited in situ. However, since POC production of both communities did not increase further at the highest light intensity (150 µmol photons m−2 s−1) even under high Fe supply, this suggests that light supply was saturated or that other conditions must be fulfilled (e.g., availability of trace metals other than Fe) in order for the communities to benefit from the higher light and Fe conditions.

The carbon stability and energy characteristics of tea waste-derived biochar: Effects of pyrolytic temperature and co-pyrolysis with nanoscale zero-valent iron

Pyrolytic temperature and Fe addition are two typical factors widely used for modifying the characteristic of biochar, however, their co-effect on the C emission reduction (enhancing C stability) and fuel features of tea waste biochar remain unclear. Hence, this study systematically investigated the effects of pyrolytic temperature (300–900 °C) and nanoscale zero-valent iron (Fe) co-pyrolysis on the C stability and fuel features of TBC. Herein, H/C, (O + N)/C, FTIR spectrum, XRD spectrum, Ig/(Id + Ig) and DOC release suggested that pyrolytic temperature improvement decreased the aliphaticity, polarity and DOC content, but increased the aromaticity and graphitic degree for TBC. Meanwhile, Fe co-pyrolysis decreased the polarity and enhanced the graphitic degree of TBC at 800–900 °C. Thermogravimetric analysis indicated that Fe co-pyrolysis lowered the thermostability of C. Differently, H2O2 oxidization method indicated Fe co-pyrolysis significantly enhanced the chemical stability of C. Furthermore, Uv–vis and fluorescence spectrum indicated that pyrolytic temperature improvement decreased the aromaticity and molecular size of biochar-derived DOC. Fe co-pyrolysis increased the release of large molecular humic-like matters rather than small molecular protein-like matters. All the results suggested high pyrolytic temperature and Fe co-pyrolysis could improve the environmental (physico-chemical) C stability of TBC and the C emission reduction. Additionally, TBC presented a considerable energy densification ratio (EDR) ranges (1.355–1.450) of wood- and straw-derived biochars, indicating TBC could be a potential high-performance biofuel to alleviate the energy crisis. This study provides important information to optimize pyrolysis conditions to re-use of tea waste for C emission reduction and fuel substitute.

Temperature-enhanced effects of iron on Southern Ocean phytoplankton

Abstract. Iron (Fe) is a key limiting nutrient for Southern Ocean phytoplankton. Input of Fe into the Southern Ocean is projected to change due to global warming, yet the combined effects of a concurrent increase in temperature with dissolved Fe (dFe) addition on phytoplankton growth and community composition have not been extensively studied. To improve our understanding of how Antarctic phytoplankton communities respond to Fe and enhanced temperature, we performed four full factorial onboard bioassays under trace-metal-clean conditions with phytoplankton communities from different regions of the Weddell Sea and the Amundsen Sea in the Southern Ocean. Treatments consisted of 2 nM Fe addition with 2 °C warming (TF), Fe addition at in situ temperature (F) +2 °C warming with no Fe addition (T) and a control at in situ temperature with no Fe addition (control, C). Temperature had a limited effect by itself but boosted the positive response of the phytoplankton to Fe addition. Photosynthetic efficiency, phytoplankton abundances and chlorophyll a concentrations typically increased (significantly) with Fe addition (F and/or TF treatment), and the phytoplankton community generally shifted from haptophytes to diatoms upon Fe addition. The < 20 µm phytoplankton fraction displayed population-specific growth responses, resulting in a pronounced shift in community composition and size distribution (mainly towards larger-sized phytoplankton) for the F and TF treatments. Such a distinct enhanced impact of dFe supply with warming on Antarctic phytoplankton size, growth and composition will likely affect trophic transfer efficiency and ecosystem structure, with potential significance for the biological carbon pump.

Modifying Microstructure and Improving Mechanical Properties of New Ti-Al-V Titanium Alloys via Fe Addition.

A comprehensive study was carried out to investigate the effects of Fe addition (0-0.9 wt.%) on the microstructure evolution and mechanical properties of Ti-6Al-4V alloys. The results indicate that Fe addition has a significant refinement effect on the microstructure of titanium alloys; specifically, 0.9 wt.% Fe addition can lead to a 47.37% decrease in the width of lamellar α. The modulus also decreases by 18.89% with the increase in the Fe content, being 91.40 GPa in Ti-6Al-4V-0.9Fe. And the microhardness and wear resistance are improved due to Fe addition. In addition, the constitutive equation of the Fe content and the elastic compliance coefficient were calculated, which can better describe the relationship between Fe addition and the elastic-plastic properties of titanium alloys. The slip systems' activity during the deformation process was also discussed using the Schmid factor. It shows that Fe addition is beneficial for the activity of prismatic and pyramidal slip systems, especially in the {101¯0} <112¯0>, {101¯1} <112¯3>, and {112¯2} <112¯3> slip systems.

Cooling Rate and Compositional Effects on Microstructural Evolution and Mechanical Properties of (CoCrCuTi)100-xFex High-Entropy Alloys.

This study investigates the impact of cooling rate and alloy composition on phase formations and properties of (CoCrCuTi)100-xFex (x = 0, 5, 10, 12.5, 15) high-entropy alloys (HEAs). Samples were synthesized using arc-melting and electromagnetic levitation, followed by quenching through the use of a Cu chill or V-shaped Cu mold. Cooling rates were evaluated by measuring dendrite arm spacings (DASs), employing the relation DAS = k ɛ-n, where constants k = 16 and n = ½. Without Fe addition, a microstructure consisting of BCC1 + BCC2 phases formed, along with an interdendritic (ID) FCC Cu-rich phase. However, with the addition of 5-10% Fe, a Cu-lean C14 Laves phase emerged, accompanied by a Cu-rich ID FCC phase. For cooling rates below 75 K/s, alloys containing 10% Fe exhibited liquid phase separation (LPS), characterized by globular Cu-rich structures within the Cu-lean liquid. In contrast, for the same composition, higher cooling rates of 400-700 K/s promoted a dendritic/interdendritic microstructure. Alloys with 12.5-15 at. % Fe displayed LPS irrespective of the cooling rate, although an increase in uniformity was noted at rates exceeding 700 K/s. Vickers hardness and fracture toughness generally increased with Fe content, with hardness ranging from 444 to 891 HV. The highest fracture toughness (5.5 ± 0.4 KIC) and hardness (891 ± 66 HV) were achieved in samples containing 15 at. % Fe, cooled at rates of 25-75 K/s.

Optimized Dehydrogenation of Magnesium Hydride with Fe and Cu Additives

Solid state hydrogen storage with the use of MgH2 has gained widespread attention because of its good reversible storage capacity. This metal hydride however slowly releases hydrogen at high temperatures ranging between 325 – 375 oC. An important feature required of MgH2 is its ability to commence hydrogen release at a fast rate and reduced temperature. Transition metal-containing alloys/compounds having either Fe or Cu as the principal element have been used to improve the dissociation of hydrogen from MgH2. Studies involving the use of each metal in its elemental form as an additive are minimal. This study investigated the catalytic effects of elemental Fe and Cu on the hydrogen release performance of MgH2 for potential applications in transportation and power generation. It was observed that MgH2/Fe had a better dehydrogenation performance; the temperature of onset of MgH2/Fe and MgH2/Cu dehydrogenation were 205, and 215 oC which were 98 and 88 oC lower than that for as-received MgH2. The highest amount, 1.9 wt. % H2 was released by MgH2/Fe while 1.44 wt. % H2 was released by MgH2/Cu. The activation energy for dehydrogenation was reduced from 150.5 kJ/mol for as-received MgH2 to 89.8 and 79.8 kJ/mol in MgH2/Cu and MgH2/Fe respectively. It took 18.8 min for as-received MgH2 to commence dehydrogenation while that for MgH2/Fe and MgH2/Cu composites started from 12.2 and 13.4 min respectively. The in-situ formed Fe and Cu in MgH2 after milling acted as active catalytic sites for its improved dehydrogenation with MgH2/Fe behaving better.

Structural and Compositional Optimization of Fe-Co-Ni Ternary Amorphous Electrocatalysts for Efficient Oxygen Evolution in Anion Exchange Membrane Water Electrolysis.

Anion exchange membrane water electrolysis (AEMWE) offers a sustainable path for hydrogen production with advantages such as high current density, dynamic responsiveness, and low-cost electrocatalysts. However, the development of efficient and durable oxygen evolution reaction (OER) electrocatalysts under operating conditions is crucial for achieving the AEMWE. This study systematically investigated Fe-Co-Ni ternary amorphous electrocatalysts for the OER in AEMWE through a comprehensive material library system comprising 21 composition series. The study aims to explore the relationship between composition, degree of crystallinity, and electrocatalytic activity using ternary contours and binary plots to derive optimal catalysts. The findings reveal that higher Co and lower Fe contents lead to increased structural disorder within the Fe-Co-Ni system, whereas an appropriate amount of Fe addition is necessary for OER activity. It is concluded that the amorphous structure of Fe-Co3-Ni possesses an optimal ternary composition and degree of crystallinity to facilitate the OER. Post-OER analyses reveal that the optimized ternary amorphous structure induces structural reconstruction into an OER-favorable OOH-rich surface. The Fe-Co3-Ni electrocatalysts exhibit outstanding performances in both half-cells and single-cells, with an overpotential of 256mV at 10mAcm- 2 and a current density of 2.0 Acm- 2 at 1.89V, respectively.

Tailoring the Compositions and Nanostructures of Trimetallic Prussian Blue Analog-Derived Carbides for Water Oxidation.

The electrochemical splitting of water for hydrogen production faces a major challenge due to its anodic oxygen evolution reaction (OER), necessitating research on the rational design and facile synthesis of OER catalysts to enhance catalytic activity and stability. This study proposes a ligand-induced MOF-on-MOF approach to fabricate various trimetallic MnFeCo-based Prussian blue analog (PBA) nanostructures. The addition of [Fe(CN)6]3- transforms them from cuboids with protruding corners (MnFeCoPBA-I) to core-shell configurations (MnFeCoPBA-II), and finally to hollow structures (MnFeCoPBA-III). After pyrolysis at 800°C, they are converted into corresponding PBA-derived carbon nanomaterials, featuring uniformly dispersed Mn2Co2C nanoparticles. A comparative analysis demonstrates that the Fe addition enhances catalytic activity, while Mn-doped materials exhibit excellent stability. Specifically, the optimized MnFeCoNC-I-800 demonstrates outstanding OER performance in 1.0mKOH solution, with an overpotential of 318mV at 10mAcm-2, maintaining stability for up to 150h. Theoretical calculations elucidate synergistic interactions between Fe dopants and the Mn2Co2C matrix, reducing barriers for oxygen intermediates and improving intrinsic OER activity. These findings offer valuable insights into the structure-morphology relationships of MOF precursors, advancing the development of highly active and stable MOF-derived OER catalysts for practical applications.

Effects of Fe addition on the mechanical and corrosive properties of biomedical Co-Cr-W-Ni alloys for balloon-expandable stents

Co-20Cr-15W-10Ni (mass%, CCWN) alloy is extensively used as a platform material for balloon-expandable stents. In this study, the mechanical properties of CCWN alloy are improved following the addition of Fe, and the effects of Fe addition on the mechanical and corrosive properties of the alloy are investigated. As-cast specimens were fabricated by adding pure Fe to a commercially available CCWN alloy (base alloy) such that the resulting alloys contained 4, 6, and 8 mass% Fe. The as-cast specimens were subjected to homogenization heat treatment at 1523 K for 7.2 ks and then hot-forged at 1473 K (as-forged specimens). The as-forged specimens were cold-rolled at a reduction rate of 30% and heat-treated at 1473 K for 300 s (recrystallized specimens). The matrix of the recrystallized base- and Fe-containing alloys consisted of a single γ (face-centered cubic)-phase. The Fe-added alloys revealed precipitates composed of the η-phase (M6X-M12X-type phase, M: metallic element, X: C and/or N). The average grain size of the recrystallized base and Fe-added alloy specimens was approximately 34 μm and the amount of added Fe had no significant effect on the static recrystallization behavior of the resulting alloys. Alloys containing 6 mass% or more Fe showed improvements in strength and ductility compared with the base alloy. When the Fe-added alloys were compared, their strength decreased whereas their ductility increased when the added Fe increased. Because Fe acts as a γ-phase-stabilizing element for Co, Fe addition increases the stacking fault energy of the base alloy, resulting in the formation of the ε (hexagonal close-packed)-phase owing to the suppression of strain-induced martensitic transformation (SIMT), and improvements in ductility. No deterioration in corrosion resistance was observed following the addition of up to 8 mass% Fe to the base alloy. Based on these results, the addition of Fe to CCWN alloy may be considered an effective method to improve its mechanical properties, especially ductility, without impairing its corrosion resistance. The results of this study will be useful for the future development of Ni-free Co-Cr alloys for next-generation, small-diameter stents.

Additive manufacturing of a new titanium alloy with tunable microstructure and isotropic properties

Conventional titanium alloys have a high propensity in developing columnar grains with strong textures during additive manufacturing (AM), which causes pronounced anisotropy in mechanical properties and hampers their practical applications. In this study, a new metastable β titanium alloy with high Fe addition (Ti-3Al-6Fe-6V-2Zr, wt.%) was designed for AM, and the strategies and underlying mechanisms to eliminating the structural heterogeneity including grain morphology, Fe element segregation and phase constituent distribution were elaborately investigated. It was demonstrated that the alloy has an outstanding intrinsic capability of forming equiaxed grains during direct energy deposition (DED) due to the positive effect of Fe on constitutional supercooling. The final microstructure of bulk sample was determined by the directly deposited microstructure and subsequent microstructure coarsening caused by cyclic heating, and homogeneously equiaxed microstructure without texture could be achieved when the heat-affected zones can fully cover the formerly deposited layer. Despite of very high level of Fe addition, both microscale and macroscale Fe segregation were completely suppressed during DED, by taking the advantages of fast solidification rate and tailoring the heating effect between the adjacent layers. Moreover, the problem related to the heterogeneity in α phase distribution along the building direction was solved by mitigating the heat accumulation during DED. On the basis of these understandings, homogeneously equiaxed Ti3662 alloy with isotropic mechanical properties of high strength (~1200MPa) and decent ductility (~10%) was finally fabricated by DED, which stands a good chance for practical application. This study demonstrates that the special metallurgical process during AM largely expands the design space of titanium alloys on the aspects of composition and microstructure, which can be utilized to fabricate titanium alloys with desirable microstructure and excellent properties.

Impact of mechanical activation and mechanochemical activation on microstructural changes, leaching rate and leachability of natural chalcopyrite

The influence of mechanical activation (MA) and mechanochemical activation (MCA) with Fe and Fe2O3 on the microstructural changes, leachability and leaching rate of natural chalcopyrite was investigated and compared. MCA pretreatments were carried out by chalcopyrite co-milling with Fe and Fe2O3 for 20 and 50 min. The XRD analysis indicated that even after 50 min MA and MCA, constituent phases of chalcopyrite, Fe and Fe2O3 could be detectable beside the newly formed bornite. Regarding the peak broadening and peak intensity reduction, MCA generally intensified the microstructural changes of chalcopyrite in comparison with MA. The microstructural study performed by the Rietveld method also proved that all microstructural parameters changed in favor of reactivity, such that the amorphization degree and microstrain were increased to 96 % and 0.164 (%), respectively, while crystallite size was reduced to 14.6 nm after 50 min MCA of chalcopyrite with Fe2O3. It could be concluded from the leaching tests that MCA along with Fe and Fe2O3 addition could promote the leachability and leaching rate of chalcopyrite, as compared to MA and nonactivated chalcopyrite. Although both the MCA of chalcopyrite with Fe and Fe2O3 could enhance copper extractions in the 1 M sulfuric acid leaching tests at 80 °C, Fe addition was slightly more effective than Fe2O3. The results obtained from the kinetic study also revealed that the leaching mechanism of nonactivated chalcopyrite, mechanically activated chalcopyrite and mechanochemically activated chalcopyrite with Fe2O3 changed from diffusion control to chemical control due to MCA with Fe. Finally, the combination of kinetic and microstructural studies proved that all microstructural parameters, except for the microstrain parameters of chalcopyrite MCA with Fe2O3, could be effective in chalcopyrite reactivity promotion.

Evaluation of leaching parameters for dissolving Ni and Co from chromite overburden using acidophilic bacterial consortium

ABSTRACT The chromite mine of Sukinda Valley located in the Indian state Odisha produces a large amount of overburden during the mining of chromite ore. The overburden waste contains different valuable metals with very low concentrations. Its environmental metal leaching contaminates nearby water resources, which creates serious chaos in the local communities. However, the presence of Ni-oxide in the overburden makes it the only Ni resources of India. Therefore, an experimental attempt was made to evaluate the possibility of Ni recovery from the overburden. The physico-chemical analysis of the overburden sample showed that it contains 0.89 and 0.031% (w/w) of Ni and Co, respectively, which remain embedded within the goethite matrix. Bioleaching may be suitably applied to it. Therefore, bioleaching of Ni and Co from the overburden sample was conducted using an acidophilic bacterial consortium. Effect of leaching parameters like contact time, initial pH, temperature, Fe(II) addition, and pulp density was evaluated. Bioleaching of the overburden sample using the acidophiles was found to be effective. Further, all the leaching parameters showed positive effect on the bioleaching efficiency.

Exogenous paths regulate electron transfer enhancing sediment phosphorus immobilization

The lack of electron acceptors in anaerobic sediments leads to endogenous phosphorus release and low removal efficiency of organic pollutants. This study introduced electrodes and iron oxides into sediments to construct electron network transport chains to supplement electron acceptors. The sediment total organic carbon (TOC) removal efficiencies of closed-circuit (CC) and closed-circuit with Fe addition (CC-Fe) were estimated to be 1.4 and 1.7 times of the control. Unlike the fluctuation of phosphorus in the overlying water of the controls, the CC-Fe was stabled at 0.04–0.08 mg/L during the 84-d operation. The phosphorus in interstitial water of CC-Fe was 30 % less than in control, whereas in sediment, the redox sensitive phosphorus was increased by 14 %, indicating phosphorus was preferred to fix into sediments rather than interstitial water. This is important to reduce the risk of endogenous phosphorus returning to the overlying water. Microbial community analysis showed that the multiplication of Fonticella in CC-Fe (20 %) was 1.8-fold of control (11 %) which improved the TOC removal efficiency. While electroactive microorganisms accumulated near the electrode reduced the abundance of Fe-reducing bacteria, such as Desulfitobacterium (2.4 %), leading to better phosphorus fixation. These findings suggest a strategy for the efficient bioremediation of endogenous pollution in water, with broader implications for regulating electron transport paths and element cycles in aquatic environments.

The intracellular accumulation of iron coincides with enhanced biohydrogen production by Thermoanaerobacterium thermosaccharolyticum

The aim of this study was to investigate the effects of different doses (10–200 mg/L) of magnetite (FeO·Fe2O3), Fe0, Ni0, and FeCl3 on the efficiency of dark fermentative H2 production from cheese whey using Thermoanaerobacterium thermosaccharolyticum SP-H2. Energy conversion efficiency and hydrogen yield increased significantly by 22.7 % and 34.8 %, respectively, when 10 mg/L of magnetite was added, and hydrogenase activity increased by 23.6 % when 100 mg/L of Fe0 was added compared to the control (p < 0.001). Using scanning electron microscopy and energy dispersive X-ray spectroscopy, it was found that during the early exponential phase of hydrogen evolution, T. thermosaccharolyticum cells accumulated up to 11.2 times more Fe (up to 2.8 wt%) in the presence of optimal concentrations of Fe additives compared to the control. Intracellular iron accumulation and hydrogen yield were positively correlated with acetate concentration (p < 0.001), suggesting an efficient acetate pathway for dark fermentation. During the stationary growth phase, with almost no H2 production, the intracellular iron content decreased by up to 67.9 %. The phenomenon of changes in the amount of metal in cells, depending on the phase of hydrogen production, was demonstrated for the first time. The findings suggest that intracellular metals can be used in cell metabolism to produce H2, and the mechanisms behind this process need further investigation. Overall, this study provides valuable insights into the optimal forms and doses of metals for enhancing biohydrogen production, as well as possible research directions for the potential use of metals by microorganisms during additive-assisted dark fermentation of carbohydrate-rich wastes.

A preliminary study: Microbial electrolysis cell assisted anaerobic digestion for biogas production from Indonesian tofu-processing wastewater at various Fe additions

Tofu-processing wastewater (TPW) is very abundant in Indonesia. This study aimed to examine the impact of Fe additions (0–600 mg-FeCl3/L) on biogas yield from TPW through anaerobic digestion (AD) without and with microbial electrolysis cells (MEC). The presence of MEC in AD increased biogas yield by 14.4–114.5 %. The optimum Fe addition either in AD or MEC-AD was 400 mg-FeCl3/L. Prediction accuracy was higher for the modified Gompertz model compared to first-order and modified Logistic models because it had a higher R2 (0.9942). The presence of MEC in AD increased ym, μ, and λ values. MEC-AD resulted in pollutant removal efficiencies 1.09 to 1.63 times higher than AD. Based on energy analysis, AD and MEC-AD resulted in surplus energy of 3582.1 and 5325.1 J, respectively. It means that the presence of MC in AD successfully increased the surplus energy by about 1.5 times.

Activating Fenton-like reaction by hydrochars containing persistent free radicals derived from various pomelo peel components

To reveal the influence of the diversity of precursors on the formation of environmental persistent free radicals (EPFRs), pomelo peel (PP) and its physically divided portion, pomelo cuticle (PC), and white fiber (WF) were used as precursors to prepare six hydrochars: PPH-Fe, PCH-Fe, WFH-Fe, PPH, PCH, and WFH with and without Fe(III) addition during hydrothermal carbonization (HTC). PPH-Fe and WFH-Fe had higher EPFRs content (9.11 × 1018 and 8.25 × 1018 spins·g−1) compared to PPH and WFH (3.33 × 1018 and 2.96 × 1018 spins·g−1), indicating that iron-doping favored EPFRs formation. However, PCH-Fe had lower EPFRs content (2.78 × 1018 spins·g−1) than PCH (7.95 × 1018 spins·g−1), possibly due to excessive iron leading to the consumption of the generated EPFRs. For another reason, the required Fe(III) amount for EPFRs formation might vary among different precursors. PC has a lower concentration of phenolic compounds but 68–97% fatty acids, while WF and PP are rich in cellulose and lignin. In the Fenton-like reaction, oxygen-centered radicals of hydrochar played a significant role in activating H2O2 and efficiently degrading bisphenol A (BPA). Mechanisms of reactive oxygen species (ROS) generation in hydrochar/H2O2 system were proposed. EPFRs on hydrochar activate H2O2 via electron transfer, creating ·OH and 1O2, leading to BPA degradation. More importantly, the embedded EPFRs on the hydrochar's inner surface contributed to the prolonged Fenton-like reactivity of PPH-Fe stored for 45 days. This study demonstrates that by optimizing precursor selection and iron doping, hydrochars can be engineered to maximize their EPFRs content and reactivity, providing a cost-effective solution for the degradation of hazardous pollutants.Graphical abstract

Fe oxides simultaneously improve stability of Cd and carbon in paddy soil：The underlying influence at aggregate level

Iron (Fe) oxides have a strong adsorption affinity for Cd and organic carbon (SOC). However, under alternate wet-dry (IF) condition,the influences of Fe oxides on the speciation and disrtribution of Cd and SOC in soil aggregates are unkown. In the present study, soils untreated (S), removed (S-Fe) or added (S+Fe) Fe oxide soils were blended with cadmium chloride solution and cultivated for 56 days under different moisture management practices. Compared with the S-Fe soil, the IF treatment increased the contents of Fe oxide-bound SOC (Fe-OC) and Fe/Mn oxide-bound Cd (Fe/Mn-Cd) by 18.5–29.8-fold and 1.45–2.45-fold, repectively, in the S and S+Fe soils, corresponding to a 36 %−42 % increase in the recalcitrant C pool (RCP) and a 53 %−87 % decrease in the exchangeable Cd content. These results could be attributed to soil particle aggregation and Fe redistribution. Fe addition promoted the transfer of Cd/SOC accumulated in microaggregates to macroaggregates and increased the variable negative charge content in macroaggregates and the adsorption capacity of macroaggregates for Cd/SOC. More Cd/SOC accumulated in macroaggregates in Fe oxide-bound form, which reduced the risk of Cd migration and Cd availability and increased the physical protection of SOC. Therefore, Fe oxide has great potential to simultaneously reduce carbon emissions and cadmium toxicity in paddy soil.

Decreased Metal Dusting Resistance of Ni-Cu Alloys by Fe and Mn Additions

Ni-Cu alloys are promising for application at temperatures between 400–900 °C and reducing atmospheres with high C-contents. Typically, under such conditions, metallic materials in contact with the C-rich atmosphere are degraded by a mechanism called metal dusting (MD). Ni-Cu-alloys do not form protective oxide scales, but their resistance is attributed to Cu, which catalytically inhibits the C-deposition on the surface. Adding other alloying elements, such as Mn or Fe, was found to enhance the MD attack of Ni-Cu alloys again. In this study, the effect of the Mn and Fe is divided into two affected areas: the surface and the bulk. The MD attack on binary Ni-Cu alloys, model alloys with Fe and Mn additions, and commercial Monel Alloy 400 is experimentally demonstrated. The surface electronic structure causing the adsorption and dissociation of C-containing molecules is investigated for model alloys. Analytical methods such as scanning electron microscopy combined with energy-dispersive X-ray spectroscopy, electron probe microanalysis combined with wavelength-dispersive X-ray spectroscopy, X-ray diffraction analysis, and near-edge X-ray absorption fine structure measurements were used. The results are correlated to CALPHAD calculations and atomistic simulations combining density functional theory calculations and machine learning. It is found that the Cu content plays a significant role in the surface reaction. The effect of Mn and Fe is mainly attributed to oxide formation. A mechanism explaining the enhanced attack by adding both Fe and Mn is proposed.

Effect of Fe addition on corrosion behavior of Ni–xFe–5Cr alloys at 570°C in air containing salt vapor

Effect of Fe addition on corrosion behavior of Ni–<i>x</i>Fe–5Cr alloys at 570°C in air containing salt vapor