Adsorption Oxidation Research Articles

Favorable Adsorption and Detection Properties of Metal Oxides (NiO and Ag₂O) Modified Janus SnSSe Monolayer Toward SF₆ Decomposition Gases in a Gas-Insulated Equipment

Favorable Adsorption and Detection Properties of Metal Oxides (NiO and Ag₂O) Modified Janus SnSSe Monolayer Toward SF₆ Decomposition Gases in a Gas-Insulated Equipment

High-performance cellulose acetate fibers-loaded Al ca layered double oxide adsorbents towards efficient elimination of anionic pollutants: Mechanism adsorption and RSM-CCD approach

High-performance cellulose acetate fibers-loaded Al ca layered double oxide adsorbents towards efficient elimination of anionic pollutants: Mechanism adsorption and RSM-CCD approach

Achieving Ultra-Low-Sulfur Model Diesel Through Defective Keggin-Type Heteropolyoxometalate Catalysts

Various Keggin-type heteropolyoxometalate catalysts with structural defects and surface acidity were synthesized by immobilizing 12-phosphotungstic acid (HPW) on mesoporous SBA−15, to produce near-zero-sulfur diesel fuel. As the calcination temperature increased, the W=O and the corner-shared W–O–W bonds in the Keggin unit partially broke, creating oxygen defects, as evidenced by the Rietveld refinement and in situ FTIR characterization. All the catalysts contained Lewis (L) and Brønsted (B) acid sites, with L acidity predominant. The relative intensity of the IR band (I980) of W=O bond inversely correlated with the number of L acid sites as the calcination temperature varied, suggesting that oxygen defects contributed to the Lewis acid sites formation. In the oxidation of dibenzothiophene (DBT) in a model diesel within a biphasic system, DBT conversion exceeded 99% under the optimal reaction conditions (reaction temperature 70 °C, reaction time 60 min, H2O2/sulfur molar ratio 8, H2O2/formic acid molar ratio 1.5, catalyst concentration 2 mg/mL). The influence of fuel composition and addition of indole and 4,6-DMDBT on DBT oxidation were also evaluated. Indole and cyclohexene negatively impacted the DBT oxidative removal. Oxygen defects served as active centers for competitive adsorption of sulfur compound and oxidant. Both L and B acid sites were involved in transferring O atom from peroxophosphotungstate complex to sulfur in DBT, resulting in DBTO2 sulfone, which was immediately extracted by polar acetonitrile. This study confirms that structural defects and surface acidity are crucial in the deep oxidative desulfurization (ODS) reaction, and in enabling the simultaneous oxidation and separation of refractory organosulfur compounds in a highly efficient model diesel.

Water-Rock Interaction Mechanisms and Hydrochemical Evolution in the Underground Reservoirs of Coal Mines.

Coal-mine underground reservoirs play pivotal roles in water purification through water-rock interactions; however, underlying mechanisms associated with water-rock interactions remain unclear to date. To address this issue, this study considered the underground reservoirs of the Daliuta coal mine, Shendong to conduct the analysis. Through onsite sampling and laboratory simulation experiments, along with hydrochemical-diagram-based analysis, multivariate statistical analysis, and hydrogeochemical simulations, the sources and evolutions of major ions associated with the water of the underground reservoirs were elucidated. Results revealed that the suspended-solid content, turbidity, electrical conductivity, and total dissolved solid concentration in the water at the outlet of the underground reservoirs decreased significantly compared to corresponding values at the inlet. Alteration in the hydrochemical type of water was observed from the Cl·HCO3-Na·Ca, Cl-Na·Ca·Mg, and Cl·SO4-Na types at the inlet of the reservoirs to SO4·Cl-Na at the outlet of the reservoirs. Further, the primary hydrogeochemical processes carried out along the water flow path in the underground reservoirs included mineral dissolution (including halite, silicate, calcite, gypsum, and anhydrite dissolution), pyrite oxidation, cation exchange, and clay-mineral adsorption. Water-rock interactions in the underground reservoirs can be categorized into three stages. The first stage was dominated by dissolution and oxidation, resulting in decreased water pH and overall increased concentrations of total dissolved solids along with major ions in the water. The second stage was dominated by clay-mineral adsorption and cation exchange, resulting in increased water pH and overall concentrations of Na+ and K+ as well as decreased concentrations of Ca2+, Mg2+, and total dissolved solids in the water body. The third stage was characterized by weak water-rock interactions, wherein the concentrations of total dissolved solids along with major ions, as well as the pH of the water stabilized. Thus, our research findings provide important theoretical references for understanding water-purification mechanisms and water-storage-duration optimization in coal-mine underground reservoirs.

Selenocyanate removal using combined system of TiO2- photocatalysis and Fe(III)/SiO2 adsorption {UV-TiO2/[Fe(III)/SiO2]}: Complex destruction and simultaneous selenium species adsorption

Selenocyanate (SeCN‾) species, commonly found in industrial effluents from crude oil refineries and mining operations, present substantial health risks to humans and animals. This study investigates the treatment of selenocyanate-contaminated streams using a combination of TiO2 photocatalysis and Fe(III)/SiO2 binary oxide adsorption {UV-TiO2/[Fe(III)/SiO2]}. The Fe(III)/SiO2 binary oxide was synthesized and characterized using X-ray diffraction (XRD) and Fourier Transform Infrared (FTIR) spectroscopy. XRD analysis revealed non-crystalline Fe-oxide phases, while FTIR indicated the presence of various Fe and O functional groups on the Fe(III)/SiO2 surface. Adsorption studies using Fe(III)/SiO2 showed its selenocyanate uptake capacity ∼ 2.1 mg/g, with the respective data closely aligning with the Langmuir isotherm model. This Fe(III)/SiO2 adsorption feature was successfully combined in the {UV-TiO2/[Fe(III)/SiO2]} system in which the hydroxyl radicals (●OH) generated by the UV-TiO2 facilitated the breakdown of the selenocyanate complex, while the resulting selenite and selenate were simultaneously adsorbed by the Fe(III)/SiO2 within a 240-min reaction time. A mathematical model developed using a face-centered central composite design-response surface methodology (FCD-RSM) showed significant predictive capability with an insignificant lack of fit. Optimal conditions for selenium removal were determined to be 20 mg/L selenocyanate, 1 g/L TiO2, and 1 g/L Fe(III)/SiO2, at pH 5, within a 240-min reaction time. Kinetic analysis demonstrated that selenocyanate degradation followed pseudo-first-order kinetics, while total selenium removal adhered to pseudo-second-order kinetics, confirming the proposed selenium species removal mechanism. Overall, this integrated approach offers a promising solution for effective selenocyanate remediation in industrial wastewater.

Removal of arsenic from aqueous solution using magnetic biochar derived from Spirulina platensis

Arsenic contamination in surface waters and groundwater affects millions of people on a daily basis. Oxidation of As(III) to less toxic As(V) is a widely used strategy to enhance the removal of As from solution. This study developed and evaluated a Fe-modified biochar (FeSP600). Spirulina platensis (SP) is one of the most promising microalgae because of its physicochemical properties and potential applications. The high N content of SP may affect the physicochemical properties of the biochar, which could be used as an inherent N source for N doping biochar by carbonization. After Fe modification, the formed Fe species and N-containing components of SP were used to introduce pyridinic N, which can be coordinated with Fe to form Fe-N. We demonstrated that the formed Fe species (Fe0, Fe2+ and Fe3+) and the defective structures in FeSP600 could act as active sites for surface catalytic reactions. FeSP600 not only had magnetic properties but also could effectively remove As from an aqueous solution. These properties were attributed to the release of Fe2+ and the reactive oxygen species (ROSs) generated by the γ-Fe2O3 particles on the crystalline defect structure. As(III) and As(V) removal were affected by the initial pH values. The removal efficiencies for As(III) increased from 57.2 % to 94.9 % as the pH increased from 3 to 9, whereas that for As(V) decreased from 80.1 % to 46.8 %. The presence of coexisting ions either completely (PO43−) or partially (Cl−, CO32− and SO42−) inhibited As removal. The removal of As(V) depended on electrostatic interactions, but As(III) removal was a complex process, including both oxidation and surface adsorption, as the ROSs were able to oxidize As(III) to As(V). Our study demonstrates that FeSP600 has properties that are beneficial for the removal of As(III) and As(V) from aqueous environments. The findings of this study have potential for real-world application in treating As-contaminated water sources, particularly in improving drinking water purification systems in developing countries. More importantly, an assessment of the impact of FeSP600 usage on aquatic ecosystems is required to ensure the safe application of this technology. Therefore, developing methods for mass production of FeSP600 is essential for the commercialization of this technology, necessitating process engineering studies in this area.

Insights into the relationship between Nitrilotri(methylphosphonic acid) (NTMP) adsorption and physicochemical properties of iron oxides

Non-reactive phosphorus (e.g., phosphonate) contributes to eutrophication, while little attention has been paid to its control. The iron-based materials are highly efficient in orthophosphate removal from water, while the correlation between their physicochemical properties and selective phosphonate (e.g. Nitrilotri(methylphosphonic acid) (NTMP)) adsorption is still unclear. In this study, Fe3O4 (magnetite), FeOOH (goethite) and Fe2O3 (hematite) with different crystal structures, particle sizes and surface area were synthesized for NTMP adsorption. The physicochemical properties of the three kinds of iron oxides were characterized. The batch experiments were applied to explore the NTMP adsorption and desorption performance. The maximum adsorption capacity of NTMP on Fe3O4, FeOOH and Fe2O3 were 4.14, 1.91 and 0.99 mg-P/g, respectively. Results implied the crystal structure and surface area of iron oxides determined the maximum NTMP adsorption capacity. The NTMP adsorption on the three iron oxides was spontaneous, endothermic and randomness increase. The iron oxides showed high selectivity towards NTMP adsorption in water containing anions, while the co-existing Ca2+ and Mg2+ remarkably increased the adsorption capacity. The successive adsorption-desorption cycles suggested a favorable reusability of the above iron oxides and a high NTMP desorption efficiency. The specific NTMP adsorption capacity followed the sequence of FeOOH > Fe2O3 > Fe3O4, and was highly dependent on surface OH− proportion. The NTMP adsorption mechanism was mainly attributed to inner-sphere complexation. This study provides insights into the iron-based adsorbents design for selective phosphonate adsorption in the future.

Preparation of printing and dyeing sludge biochar/macromolecule polymer microsphere as a non-sacrificial persulfate activator with excellent reusability and reduced heavy metals leaching

Biochar-based environmental functional materials offer a promising approach for the resourceful utilization of printing and dyeing sludge (PADS). However, pollutant desorption and heavy metal leaching pose potential environmental risks. In this study, we developed a novel PADS biochar (PADSBC) macromolecule polymer microsphere with outstanding reusability and stability. This microsphere effectively activated peroxymonosulfate (PMS) for the degradation of sulfadiazine (SDZ) while significantly reducing heavy metal leaching compared with PADSBC. The SDZ removal efficiency was not influenced by the type of macromolecule polymers (calcium alginate (CA), cellulose nanofibers (CNF), and polyvinyl alcohol (PVA)) incorporated into PADSBC. In the CA-PADSBC800 microsphere/PMS system, 97 % of SDZ was removed within 40 min, primarily through 1O2-induced oxidative degradation (62 %) and adsorption by CA-PADSBC800 (29 %). Additionally, CA-PADSBC800 prevented SDZ desorption for over five consecutive cycles, while PADSBC800 exhibited 25 % desorption. The presence of HCO3- and humic acids slightly delayed SDZ removal, while Cl- slightly accelerated it. Doping CA, CNF, and CA + CNF into PADSBC800 reduced the leaching of Cu and Cr by over 90 %, and Ni by over 80 %, under both experimental conditions and simulated surface water and landfill leachate situations. The excellent performance of the PADSBC-macromolecule polymer microspheres was attributed to the presence of carboxyl, hydroxyl, and C = O functional groups.

WITHDRAWN: Studies on decontamination of cadmium rich water by a novel nano Iron oxide adsorbent

Synthesizing non-toxic adsorbent for abatement of hazardous pollutants from water is important to develop safe environment. In this study, nanocrystalline iron oxide particles were synthesized and utilized as effective nanoadsorbent for removing cadmium through adsorption. The as-prepared nanoadsorbent was characterized using sophisticated techniques. The objective of this study was to improve cadmium adsorption from aqueous solutions under a variety of conditions. With the help of Box-Behnken design, adsorption parameter settings were improved. Response Surface Methodology analysis was conducted to optimize the adsorption conditions, including pH, initial concentration of metal ions, and adsorbent dose. Comparisons were made between the optimal equations for linear and non-linear kinetics, along with isotherm models. Origin's curve fitting tool and the Solver add-in of Microsoft Excel are two non-linear analytical tools. The obtained results showed that the Origin curve fitting tool is superior to solver add in's error analysis method for determining isotherm parameters. The equilibrium data for cadmium removal using nano iron oxide/hydroxide adsorbent was best fitted to Langmuir isotherm model. The adsorption of cadmium was well described by the pseudo-second-order model. The study shows that the system appears to be spontaneous according to the Langmuir constant method and thermodynamic parameter via partition.

Experimental and modeling studies on char combustion under pressurized O2/H2O conditions

The desorption kinetic parameters for pressurized combustion and gasification reactions were determined based on a C++ program coupled with the Langmuir-Hinshelwood (L-H) kinetic model developed and experimental data from pressurized char combustion, and the established L-H kinetic model for pressurized char-O2/H2O combustion was refined in the current paper. The activation energy for desorption in reactions involving pressurized char-O2 and char-H2O was determined to be 250.8 kJ/mol, accompanied by a pre-exponential factor of 5.42×1010 g/(m2 s). Using this foundation, the current research conducted simulations to investigate the impacts of temperature, pressure, and H2O concentration on the oxidation adsorption rate (Rads,oxi), desorption rate (Rdes), gasification adsorption rate (Rads,gas), and the competitive influences of kinetics and diffusion processes within the pressurized char-O2/H2O combustion. The simulation results indicate a gradual increase in Rdes and Rads,gas with char conversion to reach a peak, followed by a gradual decline. Conversely, the Rads,oxi varies smoothly throughout the char conversion process. At 1673 K/1.0 MPa, the char-O2/H2O reaction rate is primarily constrained by Rads,oxi and Rads,gas, with the adsorption reaction serving as the rate-controlling step. Moreover, it was noted that a rise in pressure resulted in a linear increase in Rads,oxi, Rdes, and Rads,gas. At elevated temperatures, the impact of pressure on them becomes more noticeable. However, the introduction of H2O mitigates this effect. Elevated temperature and pressure facilitate the competition on the kinetics of char-O2 combustion for O2 diffusion, resulting in the conversion of char being more susceptible to O2 diffusion rate limitation. With the addition of 20% H2O, the competition effect was weakened. In the case of pressurized combustion involving char and O2/H2O, the char conversion is primarily constrained by the O2 diffusion rate and is scarcely influenced by the H2O diffusion rate.

Adsorption and Catalytic Reduction of Nitrogen Oxides (NO, N2O) on Disulfide Cluster Complexes of Cobalt and Iron-A Density Functional Study.

The reactivity of nitrogen oxide, NO, as a ligand in complexes with [Fe2-S2] and [Co2-S2] non-planar rhombic cores is examined by density functional theory (DFT). The cobalt-containing nitrosyl complexes are less stable than the iron complexes because the Co-S bonds in the [Co2-S2] core are weakened upon NO coordination. Various positions of NO were examined, including its binding to sulfur centers. The release of NO molecules can be monitored photochemically. The ability of NO to form a (NO)2 dimer provides a favorable route of electrochemical reduction, as protonation significantly stabilizes the dimeric species over the monomers. The quasilinear dimer ONNO, with trans-orientation of oxygen atoms, gains higher stability under protonation and reduction via proton-electron transfer. The first two reduction steps lead to an N2O intermediate, whose reduction is more energy demanding: in the two latter reaction steps the highest energy barrier for Co2S2(CO)6 is 109 kJ mol-1, and for Fe2S2(CO)6, it is 133 kJ mol-1. Again, the presence of favorable light absorption bands allows for a photochemical route to overcome these energy barriers. All elementary steps are exothermic, and the final products are molecular nitrogen and water.

Simulated sunlight-driven photocatalytic activation of peroxydisulfate by core–shell Ag@SiO2/TiO2 nanocomposite for efficient methyl orange degradation

Herein, core–shell Ag@SiO2/TiO2 nanocomposites were synthesized and applied to activate peroxydisulfate (PDS) for wastewater purification. The Ag core and Ag-doped TiO2 shell were obtained by stober method and calcination method. The dispersion degree and size of Ag in TiO2 would influence the oxygen vacancy. Ag enhanced the visible absorption of TiO2 and activated PDS. Improved degradation performance was attributed to enhanced PDS activation by photogenerated e−, which separated h+and thus promoted methyl orange(MO) degradation. Reactive oxidative species were verified under dark and light conditions via quenching experiments and electron paramagnetic resonance tests, demonstrating SO4•–, h+, O2•–, and1O2were formed in light,whereasSO4•–, •OH, O2•–, and 1O2were responsible for MO degradation under dark conditions. The Ag@SiO2/TiO2/PDS/light system showed selectivity for removal of cationic dyes (e.g., methylene blue and malachite green) through adsorption and photocatalysis, whereas anionic dyes (e.g., MO) were degraded by photocatalysis alone. Besides, we found excess adsorption of micropollutant onto catalyst may be adverse to the activation of PDS. Therefore, the adsorption of oxidant (such as PDS) onto the catalyst surface would be beneficial for catalytic activation and micropollutant degradation, especially onto active sites. This work aims to provide a new avenue for core-shell structure catalyst synthesis in wastewater purification.

The Effect of CO on the Exothermic Characteristics of Low-Temperature Oxidation in Coal

ABSTRACT In recent years, abnormally high concentrations of CO gas have often been detected in goaf areas of coal mines in China, which have posed a serious threat to safe production in coal mines and the life and safety of underground personnel. The effect of CO on the exothermic characteristics of low-temperature oxidation in coal was studied by analyzing the exothermic characteristics, heat release, oxidation stages, and activation energy of coal at different CO concentrations using a C600 microcalorimeter. The experimental results indicated that CO promoted the coal oxidation at low temperature, but inhibited it after reaching 144°C. When the CO concentration is 30%, the exothermic characteristics of coal in low-temperature oxidation adsorption stage were significantly affected, with the heat flow value decreased by 27.0% and the initial exothermic temperature point moved forward by 3.9 K. In the later stage of the oxidation reaction, the heat release of coal was linearly negatively correlated with CO concentration. The higher the concentration, the lower the heat release. These findings contribute to understanding the combustion mechanism of coal in high-concentration CO atmosphere and provide valuable insights for designing and optimizing coal utilization technologies.

Reactive transport of Cd2+ in porous media in the presence of xanthate: Experimental and modeling study

In mining regions, flotation reagents can interact with heavy metals, thereby increasing the complexity of their migration. However, most current studies solely focus on the migration of heavy metals, neglecting the influence of flotation reagents in their models concerning mining area pollution. This study developed the reactive transport model, Multisurface Speciation Model (MSM), which integrated the reaction processes of the three main soil components (iron oxides, organic matter, clay minerals) and ethyl xanthate (EX), a typical flotation reagent, with cadmium (Cd²⁺) to investigate the effects of EX on the transport and retention of Cd²⁺ in natural porous media under varying pH conditions. The study revealed that EX formed new adsorption sites for Cd²⁺, enhancing its retention and inhibiting transport with increased EX loading (0 to 2.5 mmol·L−1), while higher pH levels (ranging from 4 to 8) further strengthened the retention capability of Cd²⁺. The MSM further predicted the solid-phase concentration distribution of Cd²⁺ among various components. With increasing EX-loaded concentrations, xanthate became the dominant adsorbing component, accounting for 48.93 % to 95.31 % of adsorption, and competitively interacted with other components. Xanthate retention was lower under acidic conditions compared to neutral and alkaline environments. Sensitivity analysis highlighted the concentrations of iron oxide adsorption sites (SurfaOH, SurfbOH) as critical parameters in the models, underscoring the need for precise determination of soil physicochemical indicators. This study stressed the crucial role of flotation reagents and pH conditions in controlling heavy metal mobility, offering important insights for environmental management in mining regions.

Electrosynthesis of ferrate from iron waste and seawater salts as Antibacterials for water pollutant treatment

The synthesis of ferrate from waste iron and seawater salt as antibacterial pollutants for Staphylococcus aureus and Escherichia coli in water treatment has been successfully carried out. The synthesis phases comprised the preparation of NaOCl from saltwater, Fe(OH)3 synthesis from iron waste, and the electrosynthesis of ferrate. The successful synthesis was confirmed by XRD at 30.05°, 36.87°, 40.51°, and 75.30° as Na2FeO4 (JCPDS file: 890169), the functional groups of FeO42- at 779 and 879 cm−1 in the FTIR spectrum. Moreover, it was also confirmed by the dominance of Fe and O element content in XRF and SEM-EDX, as well as the stability and ability to produce hydroxide radicals in Fluorescence analysis. Furthermore, tests of the antibacterial effectiveness were carried out with variations in doses, time observation, and method variations (agar well, disc-diffusion, and turbidimetry) using comparison variables positive control (ampicillin) and negative control (distilled water). The test results showed antibacterial ability with the inhibitory zone category “very strong” and “strong” with 100 % inhibition against E. coli bacteria 5.954 x 108 CFU/mL and 4.723 x 108 CFU/mL S. aureus. This ability increases with the dose of ferrate addition and decreases with the observation time of inactivation. Bacterial inactivation occurs through oxidation and coagulation adsorption by reactive oxygen species (ROS). E. coli is more sensitive than S. aureus due to its thinner membrane structure, allowing more manageable penetration. This research is expected to overcome the problem of iron waste while turning it into something useful as an antibacterial treatment of pollutants in the aquatic environment.

Elevating electron transfer of recyclable SERS sensor using AuNPs/TiO2/Ti3C2 heterostructures for detection of malachite green in sunfish

Malachite green (MG)-contaminated aquatic products pose a serious threat to animal and human health. Hence, a novel recyclable surface-enhanced Raman scattering (SERS) substrate based on AuNPs/TiO2/Ti3C2 heterostructures was developed for the detection and degradation of MG in aquatic products. Specifically, AuNPs/TiO2/Ti3C2 heterostructures were synthesized by in situ oxidation and electrostatic adsorption based on Ti3C2 nanosheets. The excellent photocatalytic and SERS performance of the AuNPs/TiO2/Ti3C2 was demonstrated by Density functional theory (DFT) calculations and experimental results, which was attributed to the enhancement of charge transfer (CT) after the formation of heterostructures. The results demonstrate that AuNPs/TiO2/Ti3C2 is highly sensitive and recyclable. The detection limit of the sensor for MG is 8.91 × 10−5 mg/L. The sensor can be recycled for five times under the condition of light, and shows satisfactory self-cleaning performance in the food matrix, providing a possible alternative solution for the recyclable detection of MG.

Tribological behavior of TiN, AlTiN, and AlTiCrN coatings in atmospheric and vacuum environments

In this study, the tribological characteristics of TiN, AlTiN, and AlTiCrN coatings sliding against a SUS420J1 stainless steel pin were investigated in atmospheric and vacuum environments. The coatings were deposited on SUS440C substrates using the arc-physical vapor deposition technique. The friction and wear behavior of the coatings were evaluated based on the systematic analyses of the friction coefficient data as well as the physical and chemical state of the wear track. The results revealed that the friction coefficients of the SUS440C specimen and AlTiCrN coatings increased, whereas those of the TiN and AlTiN coatings decreased when the environment was changed from atmospheric to vacuum. It was confirmed that the formation of an oxide layer and adsorption of oxides on the surface were dominant factors that influenced the tribological behavior in the atmospheric environment. On the other hand, the compatibility, oxidation inhibition, and droplets of the surface mainly affected the frictional characteristics in the vacuum environment. The results of this work are expected to aid in the selection of proper coating materials for tribological systems operating in a vacuum.

Semiconductive Tendency of the Passive Film Formed on Super Austenitic Stainless Steel SR-50A in Acidic or Alkaline Chloride Solutions

Stainless steel is widely used in various industrial fields due to its excellent corrosion resistance and mechanical properties. The key to this corrosion resistance is the thin passive film that naturally forms on the metal surface. Passive films are characterized by oxide film theory and adsorption theory, each uniquely explaining the structure and mechanism of the protective film on the metal surface. Research on the semiconductive properties of passive films on stainless steel offers diverse viewpoints, classifying theories into the point defect model and the bipolar fixed charge-induced passivity. Specific changes in passive film attributes that lead to degradation, however, are not fully understood. In this study, we analyzed the inner and outer layers of the passive film on super austenitic stainless steel SR-50A under various conditions in acidic and alkaline chloride environments. The interpretations of these results were based on the point defect model and the bipolar model for the passivation mechanism, and correlations between p-type and n-type semiconductor properties and passivation behavior were examined. The surface of the stainless steel forms a passive film comprising two layers with p-type and n-type semiconductive properties, independent of the pH of the solutions. The corrosion resistance increases as the p-type and n-type semiconductive tendencies become more balanced, consequently enhancing the properties of the passive film.

Adsorption of cadmium ion from water by using non-toxic iron oxide adsorbent; experimental and statistical modelling analysis

Adsorption of cadmium ion from water by using non-toxic iron oxide adsorbent; experimental and statistical modelling analysis

Molecular characterization on the fractionation of organic phosphorus induced by iron oxide adsorption using ESI-FT-ICR MS

The interaction between organic phosphorus (OP) and iron oxide significantly influences the phosphorus cycle in the natural environment. In shallow lakes, intense oxidation-reduction fluctuations constantly alter the existing form of iron oxides, but little is known about their impact on the adsorption and fractionation of OP molecules. In this study, electrospray ionization coupled with Fourier transform ion cyclotron resonance mass spectrometry (ESI-FT-ICR MS) was used to investigate the fractionation of OP from alkali-extracted sediment induced by crystalline goethite and amorphous ferrihydrite adsorption at a molecular scale. The results showed that ferrihydrite and goethite both exhibited high OP adsorption, and the adsorption amount decreased as the pH increased. The adsorption kinetics matched the pseudo-second-order equation. The ESI-FT-ICR MS analysis showed that 91 P-containing formulas were detected in the alkaline-extracted sediment solution. Ferrihydrite and goethite adsorbed 51 and 24 P-containing formulas, respectively, with adsorption rates of 56.0 % and 26.4 %. Ferrihydrite could adsorb more OP compounds than goethite, but no obvious molecular species selectivity was observed during the adsorption. The P-containing compounds, including unsaturated hydrocarbons-, lignin/carboxyl-rich alicyclic molecule (CRAM)-, tannin-, and carbohydrate-like molecular compounds, were more suitable for iron oxide adsorption. The double bond equivalence (DBE) is a valuable parameter that indicates OP fractionation during adsorption, and P-containing compounds with lower DBE values such as lipid- and protein-like molecular were prone to remain in the solution after adsorption. These research results provide insights into the biogeochemical cycling process of P in the natural environment.