Search Results (82)

During the high-temperature preparation of stainless steel cladding plate, carbon atoms from carbon steel diffused into stainless steel. When temperatures were within 450–850 °C, carbides precipitated at grain boundaries, which initiated intergranular sensitization and thereby reduced the corrosion resistance of stainless steel. This study designed NiP and NiCuP interlayer alloys to effectively block carbon diffusion in stainless steel cladding plates. The effect of adding interlayers on the microstructure of stainless steel cladding plate was studied by using optical microscopy and scanning electron microscopy. Electrochemical tests were subsequently conducted to evaluate the impact of interlayer incorporation on the corrosion resistance of stainless steel cladding. The results demonstrated that 304/45 specimens exhibited severe carbon diffusion, resulting in the poorest corrosion resistance. The addition of interlayers improved the corrosion resistance of stainless steel cladding to varying degrees. Among these, the 304/NiCuP/45 specimen showed the best performance. It had an intergranular corrosion susceptibility of only 0.25% and pitting potential as high as 0.336 V, which indicated its superior corrosion resistance. The passive film of stainless steel cladding exhibited n-type semiconductor characteristics. And 304/NiCuP/45 specimen demonstrated the lowest carrier density of 3.02 × 10¹⁸ cm⁻³, which indicated the formation of the densest passive film. Full article

Deep eutectic solvents (DESs) are environmentally friendly solvents formed by combining hydrogen bond donors and acceptors, resulting in a eutectic mixture with a lower melting point than the individual components. While there is extensive research on the electrochemical synthesis of platinum nanoparticles in DESs, to the best of our knowledge, there are no studies on the chemical reactivity of platinum(II) complexes in these systems. This study investigates the simple model reaction between K₂PtCl₄ and ethylenediamine (en), exploring the behaviour in DES environment, to optimize the synthesis of simple cisplatin-like platinum compounds with the potential objective of improving the traditional methods, decreasing the number of steps required for obtaining target compounds and reducing chemical waste. The reactions were performed in two hydrophilic DESs: choline chloride:glycerol 1:2 (glyceline, GL) and choline chloride:ethylene glycol 1:2 (ethaline, EG). The experiments, conducted in a 70% (v/v) DES and 30% 1:1 H₂O/D₂O mixture to allow for direct NMR analysis, revealed that en quickly formed [PtCl₂(en)], which further reacted to produce [Pt(en)₂]Cl₂. Reaction products were characterised by 1D (¹H and ¹⁹⁵Pt{¹H}) and 2D ([¹H,¹³C]-HSQC and [¹H,¹⁵N]-HSQC) NMR experiments. The discolouration of solutions, due to the consumption of K₂PtCl₄, and the precipitation of the purple Magnus salt [Pt(en)₂][PtCl₄] occurred over time. The main observed difference between the two solvent mixtures was the slower reactivity in glyceline, due to the much higher viscosity of the solution. Diffusion-ordered spectroscopy (DOSY) indicated lower water mobility in DES mixtures than pure water, with the reaction products closely associated with DES molecules. Full article

The interface between dispersed compound nanoprecipitates and metal substrates can act as effective hydrogen traps, impeding hydrogen diffusion and accumulation, thus mitigating the risk of hydrogen embrittlement and hydrogen-induced coating failure. In this study, we considered the precipitation of vanadium carbide (VC) and vanadium nitride (VN) nanoprecipitates on a body-centered cubic Fe (α-Fe) substrate in the Kurdjumov–Sachs (K–S) orientation relationship. To evaluate the stability and hydrogen trapping ability of the interface, we used the first-principles method to calculate the interfacial binding energy and hydrogen solution energy. The results show that the stability of the interface was related to the type and length of bonding between atoms at the interface. The interface zone and the interface-like Fe zone have the best hydrogen trapping effect. We found that hydrogen adsorption strength depends on both the Voronoi volume and the number of coordinating atoms. A larger Voronoi volume and smaller coordination number are beneficial for hydrogen capture. When a single vacancy exists around the interface region, the harder it is to form a vacancy, and the more unstable the interface becomes. In addition to the C vacancy at the Baker–Nutting relationship interface found in previous studies being a deep hydrogen trap, the Fe and V vacancies at the α-Fe/VC interface and the V and N vacancies at the α-Fe/VN interface in the K–S relationship also show deep hydrogen capture ability. Full article

This study investigates the influence of rare earth elements Ce and Y on the evolution of inclusions in T91 steel by melting experimental steels with varying Ce-Y contents in a vacuum induction melting furnace. The results show that the inclusions in the steel without rare earth are mainly composed of Mg-Al-O oxides, (Nb, V, Ti)(C, N) carbonitrides, and composite inclusions formed by carbonitrides coated oxides, and all of them have obvious edges and corners. Upon the addition of different concentrations of Ce and Y, the oxygen content in the steel significantly decreased, and the inclusions were modified into spherical rare earth oxides, sulfides, and oxy-sulfides. Additionally, no large-sized primary carbonitrides were observed. The average size of the inclusions was reduced from 2.8 μm in the non-rare-earth-added steel to 1.7 μm and 1.9 μm with rare earth addition. Thermodynamic analysis indicates that the possible inclusions precipitated in the steel with varying Ce contents include Ce₂O₃, Ce₂O₂S, Y₂O₃, Y₂S₃, and CeS. With the increase in Ce content, the rare earth inclusions Y₂S₃, Y₂O_3, and CeS can be transformed into Ce₂O₂S and Ce₂O₃. There are two kinds of reactions in the process of high-temperature homogenization: one is the internal transformation reaction of inclusions, which makes Y easier to aggregate in the inner layer, and the other is the reaction of Y₂S₃→CeS and Y₂O₃ + Y₂S₃→Ce₂O₂S due to the diffusion of Ce in the matrix to the inclusions. Combined with the mismatch analysis, it can be seen that Al₂O₃ has the best effect on the heterogeneous nucleation of carbonitrides during the solidification of molten steel. Among the rare earth inclusions, only Ce₂O₃ may become the nucleation core of carbonitrides, and the rest are more difficult to form heterogeneous nucleation. Therefore, by Ce-Y composite addition, increasing the Y/Ce ratio can reduce the formation of Ce₂O₃, which can avoid the precipitation of primary carbonitride and ultimately improve the dispersion strengthening effect. This study is of great significance for understanding the mechanism of rare earth elements in steel and provides theoretical guidance for the composition design and industrial trial production of rare earth steel. Full article

Biochar (BCH) amendments represent a valuable strategy for increasing forest carbon stock, but their effects on soil respiration of beech forests under climate change are largely unknown. We conducted a short-term mesocosm experiment investigating the impact of BCH applications (0%, 10%, 20%, and 50%, v/v) on respiration of a European beech forest soil in N-Italy. The experiment, carried out in Parma, was conducted under both ambient and modified climatic conditions, involving higher soil temperatures (c. +1 K) and reduced precipitation (−50%). The experiment was performed during autumn 2022 and repeated in spring 2023, periods representing late and early summer, respectively. Soil respiration significantly increased with BCH applications when compared to controls, irrespective of the percentage applied. The highest values were recorded in the 20% amendment, while values were significantly lower in BCH 50%, similar to those recorded in BCH 10%. Although soil respiration and soil temperature were positively correlated, no effect of simulated warming was observed. No effects of precipitation reduction were also found, despite respiration being significantly influenced by soil moisture. These results provide an initial insight into the potentially negligible impact of BCH applications on soil respiration in European beech forests under both current and future climate scenarios. Full article

In order to find the optimal heat input for simulating the welding of the coarse-grained heat-affected zone (CGHAZ) of a novel Q690 MPa V-N microalloyed medium and heavy plate, the study investigated the precipitation of V (C, N), microstructural changes, and impact toughness under five different heat inputs (E). The results show that in the CGHAZ, as the heat input increases, the dominant microstructure changes from intragranular acicular ferrite (IGAF) and lath bainitic ferrite (LBF) to polygonal ferrite (PF) and a small amount of IGAF. At the same time, the area fraction of the brittle phase martensite/austenite (M/A) constituents increased from 4.96% to 7.95% as heat input increased, and the microhardness difference between the M/A constituents and the matrix significantly increased. In addition, with the E increases, the fraction of high-angle grain boundaries (HAGBs), which can hinder crack propagation, increases from 59.2% to 62.2% and then decreases from 62.2% to 49.3%. Moreover, the impact toughness of the simulated CGHAZ of the Q690 MPa V-N microalloyed medium and heavy plate first increases from 62 J to 100 J and then decrease to 20 J. Full article

The difficulty of separating iron and manganese is a bottleneck issue in the traditional utilization process of iron manganese ore (Fe-Mn ore). In this work, ammonium polyvanadate (APV), an intermediate product in the vanadium industry, was introduced innovatively to convert the manganese-containing phase in Fe-Mn ore into manganese pyrovanadate (Mn₂V₂O₇) and iron and manganese were then separated efficiently through the acid leaching process. The migration of manganese, iron, and vanadium were systematically studied through XRD, SEM, and leaching experiments. Results show that during the mixed roasting process of Fe-Mn ore and APV, V₂O₅, the decomposition product of APV, reacts with the decomposition product of manganese minerals in Fe-Mn ore, Mn₂O₃, to produce the target product, acid-soluble Mn₂V₂O₇. Iron and silicon exist in the form of Fe₂O₃ and SiO₂ like in Fe-Mn ore. After the two-step leaching process of the sample roasted at 850 °C with n(MnO₂)/n(V₂O₅) of 2.25, the leaching ratios of manganese, iron and vanadium are 84.57%, 0.046%, and 4.68%, respectively, achieving the efficient separation of manganese with iron and vanadium. MnCO₃ obtained by carbonization and precipitation from the manganese-containing leaching solution can be used as an intermediate product of manganese metallurgy or manganese chemical industry. APV obtained by alkaline leaching and precipitation from the vanadium- and iron-containing tailing can be recycled into the roasting system as the roasting additive. The TFe content in the iron-containing tailing reaches 57.21 wt.%, which meets the requirement of iron concentrate. More than 99 wt.% of vanadium from the additive APV can be recovered and recycled back into the Fe-Mn ore utilization process by APV recycling and wastewater recycling, making the Fe-Mn ore utilization with APV roasting a green process. Full article

In situ X-ray diffraction has been used to investigate the stability of expanded austenite during annealing in vacuum for the austenitic stainless steel 316Ti, the super-austenitic stainless steel 904L, and the duplex steel 318LN. Expanded austenite has been formed using plasma immersion ion nitriding before. Time-of-flight secondary ion mass spectrometry before and after annealing yielded complementary information regarding nitrogen depth profiles and CrN precipitation using cluster analysis. The decay of expanded austenite during annealing was found to be thermally activated with an activation energy of 1.8 ± 0.3 eV, starting within five minutes at 550 °C and taking more than two hours below 450 °C. The decay occurs simultaneously throughout the whole nitrogen-containing zone—and not at the surface as during nitriding. Nitrogen diffusion occurring in parallel slightly complicates the data analysis. Further transmission electron microscopy investigations are necessary to understand the microstructure after annealing in vacuum. The limit for operating hard and wear-resistant expanded austenite layers at elevated temperatures of up to 350 °C is given, however, by nitrogen diffusion and not the decay into CrN. Full article

The development of the non-ferrous metal industry is generating increasingly large quantities of wastewater containing heavy metals (e.g., Sb). The precipitation of heavy metals by microorganisms involves complex mechanisms that require further investigation to optimize bioremediation technologies. In this study, we employed a sulfate-reducing bacteria (SRB) strain Desulfovibrio desulfuricans CSU_dl to treat the antimony (Sb)-containing wastewater; the behavior of Sb and mechanisms underlying precipitation were investigated by characterizing the precipitates. The results showed that the abiotic factors constraining SRB bacterial growth greatly affect Sb forms and precipitation. For instance, Sb precipitation maximumly occurred at pH 6 and 7, or C:N ratio of 10:1 and 40:3 for Sb(III) and Sb(V), respectively, resulting in a maximum Sb removal rate of 94%. Interestingly, we found that substantial antimonate and antimonite were adsorbed on the SRB cell surface, indicating that cell surface is a critical reaction site of Sb transformation and precipitation. Sb was adsorbed to the cell surface by C-C and C=O groups, and was further precipitated by forming Sb₂S₃ and Sb₂S₅ or was coprecipitated with the P-containing group. Partial Sb(V) reduction was also observed on the SRB cell surface. These results provided a deep insight into the Sb bio-transformation and were an advancement with respect to understanding bioremediation of Sb-contaminated wastewater. Full article

Geochemical proxies are a reliable tool in deciphering the paleoenvironment and diagenetic alteration in carbonate rock units. The Lower Cretaceous Yamama Formation (LCYF) is an important carbonate unit of the Saudi Arabia region which has been studied in detail to evaluate the paleoenvironment and diagenetic alteration through geochemical studies. This study presents new data on petrography, stable isotopes, and trace and rare-earth elements to enhance our understanding on paleoenvironments, redox conditions, and paleosalinity during the deposition of these carbonate units. Field studies show that the formation is composed of thick-to-thin-bedded limestone. Petrographic studies show that the formation is mostly composed of mudstone, wackestone, packstone, and grainstone facies. The stable isotopic values of carbon (δ¹³C V-PDB = +0.58‰ to +2.23‰) and oxygen (δ¹⁸O V-PDB = −6.38‰ to −4.48‰) are directly within the range of marine signatures. CaCO₃’s dominance over SiO₂ and Al₂O₃ indicates minimal detrital contribution during the LCYF precipitation. The REE pattern suggests coeval marine signatures which include (i) a slight LREE depletion compared to HREEs (av. Nd/Yb_N = 0.70), (ii) negative Ce anomalies (av. Ce/Ce* = 0.5), and (iii) a positive La anomaly (av. La/La* = 1.70). Micritic limestone has low Hf (bdl to 0.4 µg/g), Sc (bdl to 2.5 µg/g), and Th (bdl to 0.8 µg/g) content, which suggests negligible detrital influence. The Ce content of different facies (Ce = 1u.80 to 12.85 µg/g) suggests that their deposition took place under oxic to dysoxic conditions. However, there is moderate variation during the deposition of MF-I, with higher Ce values as compared to MF-II, MF-III, and MF-IV, which suggests that the deposition of MF-I mostly took place in anoxic to dysoxic conditions. Full article

Near-infrared light-triggered photocatalytic water treatment has attracted significant attention in recent years. In this novel research, rational sonochemical fabrication of Ag₂S/g-C₃N₄ nanocomposites with various compositions of Ag₂S (0–25) wt% was carried out to eliminate hazardous rhodamine B dye in a cationic organic pollutant model. g-C₃N₄ sheets were synthesized via controlled thermal annealing of microcrystalline urea. However, black Ag₂S nanoparticles were synthesized through a precipitation-assisted sonochemical route. The chemical interactions between various compositions of Ag₂S and g-C₃N₄ were carried out in an ultrasonic bath with a power of 300 W. XRD, PL, DRS, SEM, HRTEM, mapping, BET, and SAED analysis were used to estimate the crystalline, optical, nanostructure, and textural properties of the solid specimens. The coexistence of the diffraction peaks of g-C₃N₄ and Ag₂S implied the successful production of Ag₂S/g-C₃N₄ heterojunctions. The band gap energy of g-C₃N₄ was exceptionally reduced from 2.81 to 1.5 eV with the introduction of 25 wt% of Ag₂S nanoparticles, implying the strong absorbability of the nanocomposites to natural solar radiation. The PL signal intensity of Ag₂S/g-C₃N₄ was reduced by 40% compared with pristine g-C₃N₄, implying that Ag₂S enhanced the electron–hole transportation and separation. The rate of the photocatalytic degradation of rhodamine B molecules was gradually increased with the introduction of Ag₂S on the g-C₃N₄ surface and reached a maximum for nanocomposites containing 25 wt% Ag₂S. The radical trapping experiments demonstrated the principal importance of reactive oxygen species and hot holes in destroying rhodamine B under natural solar radiation. The charge transportation between Ag₂S and g-C₃N₄ semiconductors proceeded through the type I straddling scheme. The enriched photocatalytic activity of Ag₂S/g-C₃N₄ nanocomposites resulted from an exceptional reduction in band gap energy and controlling the electron–hole separation rate with the introduction of Ag₂S as an efficient photothermal photocatalyst. The novel as-synthesized nanocomposites are considered a promising photocatalyst for destroying various types of organic pollutants under low-cost sunlight radiation. Full article

The strengthening mechanism of Nb, V, and Nb-V micro-alloyed high-strength bolt steels was investigated and compared using microstructural evolution and strength modeling. Optical microscopy (OM), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD) were used to characterize the microstructure and precipitations. The results show that Nb-V composite micro-alloyed steel possessed a higher yield strength compared with Nb or V micro-alloyed steel when quenched at 870 °C and tempered at 450–650 °C. Furthermore, the strength increment of Nb-V micro-alloyed steel with respect to Nb or V micro-alloyed steel reached the maximum at a tempering temperature of 600 °C, and precipitation strengthening and dislocation strengthening presented higher strength contributions in Nb-V micro-alloyed steel than in Nb micro-alloyed steel and V micro-alloyed steel owing to the higher volume fraction and finer precipitate size. When V was added in combination with Nb in steel, the number of Nb-rich carbonitrides increased, which resulted in a higher volume fraction of the effective pinning particles-Nb-rich (Ti,Nb,V)(C,N) with diameters smaller than 50 nm and led to an enhanced refinement of the prior austenite grain. In addition, Nb could reduce the consumption of V during quenching, allowing more V to be solid-solved in the matrix after quenching, thereby further enhancing the precipitation strengthening effect of V during tempering. Full article

Numerical weather prediction (NWP) models are indispensable for studying severe convective weather events. Research demonstrates that the outcomes of convective precipitation simulations are profoundly influenced by the choice between single or double-moment schemes for ice precipitation particles and the categorization of rimed ice. The advancement of dual-polarization radar has enriched the comparative validation of these simulations. This study simulated a convective event in Guangdong, China, from May 7 to 8, 2017, employing two bulk microphysical schemes (Morrison and WDM6) in the WRF v4.2 model. Each scheme was divided into two versions: one representing rimed ice particles as graupel (Mor_G, WDM6_G) and the other as hail (Mor_H, WDM6_H). The simulation results indicated negligible differences between the rimed ice set as graupel or hail particles, for both schemes. However, the Morrison schemes (Mor_G, Mor_H) depicted a more accurate raindrop size distribution below the 0 °C height level. A further analysis suggested that disparities between the Morrison and WDM6 schemes could be attributed to the intercept parameter (N₀) setting for snow and graupel/hail in WDM6 scheme. The prescribed snow and graupel/hail N₀ of WDM6 scheme might influence the melting processes, leading to a higher number concentration but a reduced mass-weighted diameter of raindrops. Reducing the intercept parameter for snow and graupel/hail in the WDM6 scheme could potentially enhance the simulation of convective precipitation. Conversely, the increase in N₀ might deteriorate the precipitation simulation performance of the WDM6_G scheme, whereas the WDM6_H scheme exhibits minimal sensitivity to such changes. Full article

Thermosensitive polymers P1–P6 of N-isopropylacrylamide (PNIPA) and poly(ethylene glycol) dimethacrylates (PEGDMAs), av. Mn 550–20,000, were synthesized via surfactant-free precipitation polymerization (SFPP) using ammonium persulfate (APS) at 70 °C. The polymerization course was monitored by the conductivity. The hydrodynamic diameters (HDs) and the polydispersity indexes (PDIs) of the aqueous dispersion of P1–P6 in the 18–45 °C range, assessed via dynamic light scattering (DLS), were at 18° as follows (nm): 73.95 ± 19.51 (PDI 0.57 ± 0.08), 74.62 ± 0.76 (PDI 0.56 ± 0,01), 69.45 ± 1.47 (PDI 0.57 ± 0.03), 196.2 ± 2.50 (PDI 0.53 ± 0.04), 194.30 ± 3.36 (PDI 0.56 ± 0.04), 81.99 ± 0.53 (PDI 0.56 ± 0.01), 76.87 ± 0.30 (PDI 0.54 ± 0.01), respectively. The electrophoretic mobilities estimated the zeta potential (ZP) in the 18–45 °C range, and at 18 °C they were as follows (mV): −2.57 ± 0.10, −4.32 ± 0.67, −5.34 ± 0.95, −-3.02 ± 0.76, −4.71 ± 2.69, −2.30 ± 0.36, −2.86 ± 0.42 for polymer dispersion P1–P6. The polymers were characterized by attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FTIR), H nuclear magnetic resonance (¹H NMR), thermogravimetric analysis (TG/DTA), Differential Scanning Calorimetry (DSC), and powder X-ray diffraction analysis (PXRD). The length of the cross-linker chain influences the physicochemical properties of the obtained polymers. Full article

This study examines the microstructure, mechanical properties, and precipitation behavior of 1000 MPa grade GEN3 steel when subjected to various quenching processes, with a focus on the quench and partition (Q&P) technique. The Q&P-treated samples achieved 1300 MPa tensile strength and demonstrated superior yield strength, attributed to their refined substructure and their large amounts of precipitates. The quenched samples exhibited the thinnest martensite laths due to the highest martensite volume. Despite the as-annealed samples having the smallest grain size, the Q&P treatment resulted in optimal microstructural refinement results and a high dislocation density, reaching 1.15 × 10¹⁵ m⁻². Analysis of the precipitates revealed the presence of V₈C₇, M₇C₃, M₂C, and Ti(C, N) across various heat treatments. The application of the McCall–Boyd method and the Ashby–Orowan correction model indicated that quench and tempered (Q&T) samples contained the largest volume of fine precipitates, contributing to their high yield strengths. These findings offer valuable insights for optimizing heat treatment processes to develop advanced high-strength steels for industrial applications. Full article