Magnetic and electrochemical behavior of rhombohedral α-Fe2O3 nanoparticles with (1 0 4) dominant facets

Uniform rhombohedral α-Fe₂O₃ nanoparticles, ～60 nm in size, were synthesized via a triphenylphosphine-assisted hydrothermal method. Scanning electron micrograph (SEM) and transmission electron micrograph (TEM) analyses showed that the as-synthesized rhombohedral nanoparticles were enclosed by six (1 0 4) planes. The concentration of triphenylphosphine played an important role in morphological evolution of the α-Fe₂O₃ nanoparticles. The as-prepared rhombohedral nanoparticles possessed remanent magnetization M_r of 2.6 × 10^?3 emu/g and coercivity H_C of 2.05 Oe, both lower than those of other α-Fe₂O₃ particles with similar size, indicating their potential applications as superparamagnetic precursor materials. Furthermore, these rhombohedral α-Fe₂O₃ nanoparticles exhibited good sensor capability toward H₂O₂ with a linear response in the concentration range of 2–20 mM.     

Seasonal variations and sources of mass and chemical composition for PM10 aerosol in Hangzhou,China

Aerosol observation was conducted for four seasons from September 2001 to August 2002 at five sampling sites in Hangzhou, South China, on PM10 mass, 22 elements （Na, Mg, AI, Si, P, S, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As. Se, Br, Cd, Ba, and Pb）, 5 major ions （F^-, Cl^ , NO3^-, SO4^2- , and NH4^＋）, and organic and elemental carbon （OC and EC）, showing that PM10 mass ranged from 46.7 to 270.8 μg/m^3, with an annual average of 119.2 μg/m^3. Na, AI, Si, S, K, Ca, and Fe were the most abundant elements in PM10, most of S being in the form of SO4^2- . SO4^2-, NO3^-, and NH4^＋ were the major ions, which contributed to about 20% of the PM10 mass. The mean seasonal concentrations for SO4^2- , averaged over all sites, were found to be 18.0, 18.5, 24,Z and 21.4 μg/m^3, for spring, summer, autumn, and winter, respectively, while the corresponding loadings for NO3^- were 7.2, 4.7, 7.1, and 11.2 μg/m^3, and for NH4^＋ were 6.0, 5.9, 8.2, and 9.3 μg/m^3, in the form mostly of NH4NO3 in spring, autumn, and winter, and mostly of （NH4）2SO4 in summer. The low NO3^-/SO4^2- ratio found indicates coal combustion as the major source throughout the year. The mean annual concentrations of OC and EC in PM10 were found to be 21.4, and 4.1 μg/m^3, respectively. Material balance calculation indicated that fugitive dust, the secondary aerosol, and carbonaceous matter were the most abundant species in PM10 for the four seasons, as is characteristic for cities in South China.     

Chemical characteristics and Pb isotopic compositions of PM2.5 in Nanchang,China

In mid-September 2013, PM_2.5 samples were collected at six sites in Nanchang, Jiangxi Province, China, to quantify nine water-soluble ions (Ca²⁺, Mg²⁺, K⁺, Na⁺, NH₄⁺, SO₄²⁻, Cl⁻, F⁻, NO₃⁻), 29 trace elements (Ba, Zn, Pb, Ni, Mo, Cr, Cu, Sr, Sb, Rb, Cd, Bi, Zr, V, Ga, Li, Y, Nb, W, Cs, Tl, Sc, Co, U, Hf, In, Re, Be, and Ta), and to characterize Pb isotopic ratios (²⁰⁷Pb/²⁰⁶Pb, ²⁰⁸Pb/²⁰⁶Pb, and ²⁰⁷Pb/²⁰⁴Pb) for identifying the main source(s) of Pb. The results showed that the average daily PM_2.5 concentration (53.16 ± 24.17) μg/m³ was within the secondary level of the Chinese ambient air quality standard. The combined concentrations of SO₄²⁻, NH₄⁺, and NO₃⁻ to total measured water-soluble ion concentrations in PM_2.5 ranged from 79.40% to 95.18%, indicating that anthropogenic sources were significant. Coal combustion and vehicle emissions were both contributors to PM_2.5 based on the NO₃⁻/SO₄²⁻ ratios. Wushu School experienced the lowest concentrations of PM_2.5 and most trace elements among the six sampling sites. Enrichment factor results showed that Tl, Cr, In, Cu, Zn, Pb, Bi, Ni, Sb, and Cd in PM_2.5 were affected by anthropogenic activities. Cluster analysis suggested that Cd, Sb, Pb, Re, Zn, Bi, Cs, Tl, Ga, and In were possibly related to coal combustion and vehicle exhaust, while Ni, Nb, Cr, and Mo may have originated from metal smelting. Pb isotopic tracing showed that coal dust, cement dust, road dust and construction dust were the major Pb sources in PM_2.5 in Nanchang. Combined, these sources contributed an average of 72.51% of the Pb measured, while vehicle exhaust accounted for 27.49% of Pb based on results from a binary Pb isotope mixed model.     

Morphology and magnetic properties of α-Fe2O3 particles prepared by octadecylamine-assisted hydrothermal method

α-Fe₂O₃ particles with various morphologies, including micro-doublesphere, tetrakaidecahedron and nanoparticles-aggregated micro-ellipsoid, were successfully synthesized via an octadecylamine-assisted hydrothermal method. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM). The results indicate that the presence of octadecylamine played a crucial role in morphology evolution by selective crystal adsorption. The protonated octadecylamine increased the pH value that accelerated nucleation, and the long alkyl groups of octadecylamine acted as an adsorption inhibitor to retard the growth of nanoparticles. The as-prepared α-Fe₂O₃ particles exhibited higher remanent magnetization and coercivity than other α-Fe₂O₃ particles of similar size. These properties should be attributed to the superstructure and the shape anisotropy of the synthesized particles.     

Characterization of summer PM2.5 aerosols from four forest areas in Sichuan,SW China

Aerosol samples were collected over 24 and 12 h to represent day/night aerosol characteristics in forest areas at Ya’an Baima Spring Scenic Area (BM), Panzhihua Cycas National Nature Reserve (PZ), Gongga Mountain National Nature Reserve (GG), and Wolong National Nature Reserve (WL), during the summers of 2010–2012. Mass and chemical component concentrations, including organic carbon, elemental carbon, and inorganic ions (F⁻, Cl⁻, NO₂⁻, NO₃⁻, SO₄²⁻, C₂O₄²⁻, PO₄³⁻, K⁺, Na⁺, Ca²⁺, Mg²⁺, and NH₄⁺), of PM_2.5 aerosols were measured. The average PM_2.5 concentrations for 24 h were 72.42, 104.89, 20.55, and 29.19 μg/m³ at BM, PZ, GG, and WL, respectively. Organic matter accounted for 38.0–49.3%, while elemental carbon accounted for 2.0–5.7% of PM_2.5 mass. The sum concentrations of SO₄²⁻, NH₄⁺, and NO₃⁻ accounted for 23.0%, 17.4%, 22.1%, and 30.5% of PM_2.5 mass at BM, PZ, GG, and WL, respectively. Soil dust was also an important source of PM_2.5, accounting for 6.3%, 17.0%, 10.4%, and 19.1% of PM_2.5 mass at BM, PZ, GG, and WL, respectively. These reconstructed masses accounted for 75.9–102.0% of PM_2.5 mass from the four forest areas of SW China.     

Tribological and tribochemical properties of magnetite nanoflakes as additives in oil lubricants

This detailed the tribological and tribochemical properties of magnetite (Fe₃O₄) nanoflakes used as additives in ^#40 base oil in a four-ball tribo-tester. The average friction coefficient of the friction pair for lubricant containing the Fe₃O₄ nanoflakes of 1.5 wt% as a lubricant additive in the base oil is decreased by 18.06% compared to that of solely base oil. The chemical composition of base oil with the Fe₃O₄ nanoflake additives did not change during the 48-h friction assessment. The decreased saturation magnetization and increased coercivity of magnetite nanoflakes occurred due to the distortion of the basal planes and the presence of hematite (α-Fe₂O₃) generated by the tribochemical reactions during the friction process. The multi-layer low-shear-stress tribochemical lubrication films on the surface of the friction pair could form because the nanoflake particles arrange and adhere onto the surface of the friction pair in an orderly manner, and the tribochemical reactions of the friction pair in the presence of the nanoflakes occur as Fe → FeO → Fe₃O₄ → γ-FeOOH → γ-Fe₂O₃ → α-Fe₂O₃. The formation of the films can improve the tribological properties.     

Liquid phase heterogeneous photocatalytic ozonation of phenol in liquid–solid fluidized bed: Simplified kinetic modeling

The isotherms of original AC (activated carbon) and photocatalysts (TiO₂-AC) calcined at 500 °C for phenol were measured. The results showed a reversible adsorption of phenol onto both kinds of particles at 25 °C, and could be fitted well to the Freundlich adsorption equation for the dilute solution. Five oxidation processes, namely O₃, O₃/UV, O₃/UV/AC, O₂/UV/TiO₂ and O₃/UV/TiO₂, for phenol degradation in fluidized bed were evaluated and compared, and the photocatalytic ozonation was found to give the highest phenol conversion because of the combined actions of homogenous ozonation in the liquid phase, heterogeneous ozonation on the surface of the catalyst support, i.e. activated carbon, and heterogeneous photocatalytic oxidation on the TiO₂ catalyst surface. With the simplified kinetic model, photolytic ozonation was confirmed to predominantly take place on the particle surface in comparison with the heterogeneous and homogeneous photolytic ozonation. Additionally, the heterogeneous photocatalytic oxidation constant was found to be enhanced by 3.73 times in photocatlaytic ozonation process with ozone as the scavenger compared to the photocatalytic oxidation process with oxygen as the scavenger.     

Effect of chemical composition of PM2.5 on visibility in Guangzhou,China, 2007 spring

The object of this study was to investigate the correlation of visibility with chemical composition of PM2.5 in Guangzhou. In April 2007, 28 PM2.5 samples were collected daily at the monitoring station of the South China Institute of Environmental Sciences （SCIES）, in urban Guangzhou. Water-soluble ionic species （CI^-, NO3^-, SO4^2-, NH4^＋, K^＋, Na^＋, Ca^2＋, and Mg^2＋） and carbonaceous contents （OC and EC） of the PM2.5 samples were determined to characterize their impact on visibility impairment. The results showed that sulfate was the dominant species that affected both light scattering and visibility. The average percentage contributions of the visibility-degrading species to light scattering coefficient were 40% for sulfate, 16% for nitrate, 22% for organics, and 22% for elemental carbon. Because of its foremost effect on visibility, sulfate reduction in PM2.5 would effectively improve the visibility of Guangzhou.     

Chemical characteristics of PM2.5 during dust storms and air pollution events in Chengdu,China

Daily fine particulate (PM_2.5) samples were collected in Chengdu from April 2009 to February 2010 to investigate their chemical profiles during dust storms (DSs) and several types of pollution events, including haze (HDs), biomass burning (BBs), and fireworks displays (FDs). The highest PM_2.5 mass concentrations were found during DSs (283.3 μg/m³), followed by FDs (212.7 μg/m³), HDs (187.3 μg/m³), and BBs (130.1 μg/m³). The concentrations of most elements were elevated during DSs and pollution events, except for BBs. Secondary inorganic ions (NO₃^?, SO₄^2?, and NH₄⁺) were enriched during HDs, while PM_2.5 from BBs showed high K⁺ but low SO₄^2?. FDs caused increases in K⁺ and enrichment in SO₄^2?. Ca²⁺ was abundant in DS samples. Ion-balance calculations indicated that PM_2.5 from HDs and FDs was more acidic than on normal days, but DS and BB particles were alkaline. The highest organic carbon (OC) concentration was 26.1 μg/m³ during FDs, followed by BBs (23.6 μg/m³), HDs (19.6 μg/m³), and DSs (18.8 μg/m³). In contrast, elemental carbon (EC) concentration was more abundant during HDs (10.6 μg/m³) and FDs (9.5 μg/m³) than during BBs (6.2 μg/m³) and DSs (6.0 μg/m³). The highest OC/EC ratios were obtained during BBs, with the lowest during HDs. SO₄^2?/K⁺ and TCA/SO₄^2? ratios proved to be effective indicators for differentiating pollution events. Mass balance showed that organic matter, SO₄^2?, and NO₃^? were the dominant chemical components during pollution events, while soil dust was dominant during DSs.     

Influence of nanoparticle surface coating on pool boiling

The purpose of this work is to study the effects of nanostructured surface coatings on boiling heat transfer and CHF. Boiling experiments are performed on a 100 μm diameter platinum wire immersed in saturated water or pentane at 1 bar. Nanostructured surface coating is obtained by deposition of charged γ-Fe₂O₃ nanoparticles (average diameter of 10 nm) on the platinum wire. Two different processes are compared: vigorous boiling and electrophoresis.The deposition of nanoparticles onto the heated surface induces a significant increase of the boiling critical heat flux (CHF) related to the increase of wettability. It also induces a decrease of the heat transfer coefficient when the wire is entirely covered with nanoparticles. The critical heat flux enhancement depends on the wettability of the fluid compared with the bare heater. Different physical mechanisms are also studied to explain the evolution of the characteristic parameters of the boiling on nanostructured surfaces.     

Chemical characteristics of PM2.5 during haze episodes in the urban of Fuzhou,China

Atmospheric fine particles (PM_2.5) were collected in this study with middle volume samplers in Fuzhou, China, during both normal days and haze days in summer (September 2007) and winter (January 2008). The concentrations, distributions, and sources of polycyclic aromatic hydrocarbons (PAHs), organic carbon (OC), elemental carbon (EC), and water soluble inorganic ions (WSIIs) were determinated. The results showed that the concentrations of PM_2.5, PAHs, OC, EC, and WSIIs were in the orders of haze > normal and winter > summer. The dominant PAHs of PM_2.5 in Fuzhou were Fluo, Pyr, Chr, BbF, BkF, BaP, BghiP, and IcdP, which represented about 80.0% of the total PAHs during different sampling periods. The BaPeq concentrations of ∑PAHs were 0.78, 0.99, 1.22, and 2.43 ng/m³ in summer normal, summer haze, winter normal, and winter haze, respectively. Secondary pollutants (SO₄^2?, NO₃^?, NH₄⁺, and OC) were the major chemical compositions of PM_2.5, accounting for 69.0%, 55.1%, 63.4%, and 64.9% of PM_2.5 mass in summer normal, summer haze, winter normal, and winter haze, respectively. Correspondingly, secondary organic carbon (SOC) in Fuzhou accounted for 20.1%, 48.6%, 24.5%, and 50.5% of OC. The average values of nitrogen oxidation ratio (NOR) and sulfur oxidation ratio (SOR) were higher in haze days (0.08 and 0.27) than in normal days (0.05 and 0.22). Higher OC/EC ratios were also found in haze days (5.0) than in normal days (3.3). Correlation analysis demonstrated that visibility had positive correlations with wind speed, and negative correlations with relative humidity and major air pollutants. Overall, the enrichments of PM_2.5, OC, EC, SO₄^2?, and NO₃^? promoted haze formation. Furthermore, the diagnostic ratios of IcdP/(IcdP + BghiP), IcdP/BghiP, OC/EC, and NO₃^?/SO₄^2? indicated that vehicle exhaust and coal consumption were the main sources of pollutants in Fuzhou.     

Analyses of tensile deformation of nanocrystalline α-Fe2O3+fcc-Al composites using molecular dynamics simulations

The tensile deformation of nanocrystalline α-Fe₂O₃+fcc-Al composites at room temperature is analyzed using molecular dynamics (MD) simulations. The analyses focus on the effects of variations in grain size and phase volume fraction on strength. For comparison purposes, nanostructures of different phase volume fractions at each grain size are given the same grain morphologies and the same grain orientation distribution. Calculations show that the effects of the fraction of grain boundary (GB) atoms and the electrostatic forces between atoms on deformation are strongly correlated with the volume fractions of the Al and Fe₂O₃ phases. In the case of nanocrystalline Al where electrostatic forces are absent, dislocation emission initiates primarily from high-angle GBs. For the composites, dislocations emits from both low-angle and high-angle GBs due to the electrostatic effect of Al-Fe₂O₃ interfaces. The effect of the interfaces is stronger in structures with smaller average grain sizes primarily because of the higher fractions of atoms in interfaces at smaller grain sizes. At all grain sizes, the strength of the composite lies between those of the corresponding nanocrystalline Al and Fe₂O₃ structures. Inverse Hall-Petch (H-P) relations are observed for all structures analyzed due to the fact that GB sliding is the dominant deformation mechanism. The slopes of the inverse H-P relations are strongly influenced by the fraction of GB atoms, atoms associated with defects, and the volume fractions of the Al and Fe₂O₃ phases.     

Controlled growth of silver nanoparticles in a hydrothermal process

A two-step synthesis was used to control the shape of silver nanoparticles prepared via reduction of Ag^＋ ions in aqueous Ag（NH3）2NO3 by poly（N-vinyl-2 First, a few spherical silver nanoparticles,-10 nm in size, were pyrrolidone） （PVP）. Then, in a subsequent hydrothermal treatment, the remaining Ag^＋ ions were reduced by PVP into polyhedral nanoparticles, or larger spherical nanoparticles formed from the small spherical seed silver nanoparticles in the first step. The morphology and size of the resultant particles depend on the hydrothermal temperature, PVP/Ag molar ratio and concentration of Ag^＋ ions. By using UV-visible spectroscopy （UV-vis）, transmission electron microscopy （TEM） and powder X-ray diffraction （XRD）, the possible growth mechanism of the silver nanoparticles was discussed. 2007 Chinese Society of Particuology and Institute of Process Engineering, Chinese Academy of Sciences. Published by Elsevier B.V.     

A collisional-radiative code for computing air plasma in high enthalpy flow

A time-dependent collisional-radiative model for air plasma has been developed to study the effects of nonequilibrium atomic and molecular processes on population densities in a weakly ionized high enthalpy flow. This model consists of 15 species: e^-,N, N⁺,N²⁺,O, O⁺,O²⁺,O^-,N₂,N₂⁺,NO, NO⁺,O₂,O₂⁺{{\rm e}^{-},{\rm N, N}^{+},{\rm N}^{2+},{\rm O, O}^{+},{\rm O}^{2+},{\rm O}^{-},{\rm N}_{2},{{\rm N}_{2}}^{+},{\rm NO, NO}^{+},{\rm O}_{2},{{\rm O}_{2}}^{+}}, and O₂^-{{{\rm O}_{2}}^{-}} with their major electronic excited states. Many elementary processes are considered in the number density range of 10¹²/cm³ ≤ N ≤ 10¹⁹/cm³ and the temperature range of 300 K ≤ T ≤ 40,000 K. We then compare our results with an existing collisional-radiative code to validate our model. Additionally, the unsteady nature of pulsively heated air plasma is investigated. When the ionization relaxation time is of the same order as the time scale of a heating pulse, the effects of unsteady ionization are important for estimating air plasma states. From parametric computations, we determine the appropriate conditions for the collisional-radiative steady state, local thermodynamic equilibrium, and corona equilibrium models in that density and temperature range.     

Performance test of a shell-and-plate type evaporator for OTEC

The performance test of a shell-and-plate type evaporator (total surface area 21.95 m², length 1450 mm, width 235 mm, 100 plates) for ocean thermal energy conversion (OTEC) plants is reported. Freon 22 (R22) and ammonia (NH₃) were used as the working fluid. Empirical correlations are proposed for predicting the boiling heat transfer and the heat transfer coefficients on the water side. The water-side pressure drop is about 2.9 × 10⁴ N/m² when the warm water velocity is 0.7 m/s. The water-side friction factor is obtained.     

Modeling of catalytic activity of an Al2O3 surface on the basis of the first principles

The adsorption, desorption, impact, and associative heterogeneous recombination rate coefficients are determined for atomic oxygen in the temperature range between 500 and 2000 K on the basis of quantum chemical data on the energy of interaction of atomic and molecular oxygen with the clusters that model an α-Al₂0₃ surface. These coefficients are used to calculate the heterogeneous recombination probabilities and the heat fluxes to the surface under the conditions similar to those of the MESOX facility.     

Transport of Ca+2 and $${{\rm SO}_{4}^{-2}}$$ ions in Porous Media of Clay Product and its Association with the Efflorescence Phenomenon

This study investigates the displacement of SO₄^-2{{\rm SO}_{4}^{-2}} and Ca⁺² ions in a red-clay ceramic, simulating the process of efflorescence. Ceramic bodies were molded (70 × 27 × 9 mm³) by vacuum extrusion formulated with different contents of CaSO₄ · 2H₂O (0, 2, 4, 8, and 16% in weight) and burnt at different temperatures (800, 850, 900, and 950°C) for 12 h. Ceramic bodies were characterized in terms of water absorption, apparent porosity, and pore size distribution. Efflorescence was evaluated according to the norms of ASTM C67/2003 and by testing the solubilization of SO₄^-2{{\rm SO}_{4}^{-2}} and Ca⁺² ions after 1 h with the ceramic bodies immersed in hot water as well as after 7, 14, and 28 consecutive days with the ceramic bodies immersed in cold water. In the quantification of efflorescence, a new image analysis methodology was developed by using the graphic software Image Tools 3.0. The results allowed in establishing a relationship between the efflorescence of the investigated ions, physical properties (water absorption and apparent porosity), pore size distribution, and solubilization.     

Transport of Ca+2 and $${{\rm SO}_{4}^{-2}}$$ Ions in Porous Media of Clay Product and Its Association with the Efflorescence Phenomenon

This study investigates the displacement of SO₄^-2{{\rm SO}_{4}^{-2}} and Ca⁺² ions in a red-clay ceramic, simulating the process of efflorescence. Ceramic bodies were molded (70 × 27 × 9mm³) by vacuum extrusion formulated with different contents of CaSO₄· 2H₂O (0, 2, 4, 8, and 16% in weight) and burnt at different temperatures (800, 850, 900, and 950°C) for 12 h. Ceramic bodies were characterized in terms of water absorption, apparent porosity and pore size distribution. Efflorescence was evaluated according to the norms of ASTM C67/2003 and by testing the solubilization of SO₄^-2{{\rm SO}_{4}^{-2}} and Ca⁺² ions after 1 h with the ceramic bodies immersed in hot water as well as after 7, 14, and 28 consecutive days with the ceramic bodies immersed in cold water. In the quantification of efflorescence, a new image analysis methodology was developed by using the graphic software Image Tools 3.0. The results allowed in establishing a relationship between the efflorescence of the investigated ions, physical properties (water absorption and apparent porosity), pore size distribution, and solubilization.     

Interaction between SO2 from flue gas and sorbent particles in dry FGD processes

Among the technologies to control SO₂ emission from coal-fired boilers, the dry flue gas desulphurization (FGD) method, with appropriate modifications, has been identified as a candidate for realizing high SO₂ removal efficiency to meet both technical and economic requirements, and for making the best quality byproduct gypsum as a useful additive for improving alkali soil.Among the possible modifications two major factors have been selected for study:

• (1)favorable chemical reaction kinetics at elevated temperatures and the sorbent characteristics;
• (2)enhanced diffusion of SO₂ to the surface and within the pores of sorbent particles that are closely related to gas-solid two-phase flow patterns caused by flue gas and sorbent particles in the reactor.

To achieve an ideal pore structure, a sorbent was prepared through hydration reaction by mixing lime and fly ash collected from bag house of power plants to form a slurry, which was first dewatered and then dried. The dry sorbent was found capable of rapid conversion of 70% of its calcium content at 700^oC, reaching a desulphurization efficiency of over 90% at a Ca/S ratio of 1.3.Experiments confirmed that the diffusion effect of SO₂ is an important factor and that gas-solid two-phase flow plays a key role to mixing and contact between SO₂ and sorbent particles. For designing the FDG reactor, a new theoretical drag model was developed by combination of CFD with the Energy Minimization Multi-Scale (EMMS) theory for dense fluidization systems. This new drag model was first verified by comparing calculated and measured drag values, and was then implemented in simulation of gas-solid two-phase flow in two circulating fluidized beds with different sizes and flow parameters. One riser has diameter and height of 0.15m×3m and another one 0.2m×14.2m. Their superficial gas velocities are 4 and 5.2m·s⁻¹, respectively, and the circulating rate 53 and 489 kg·(m⁻²·s⁻¹). FCC particles were used in both cases. The results show that not only the static pressure drop along the riser height, but also radial distributions of particle volume fraction have been very well predicted in comparison with experiments. The new drag model is expected to shed more light on the further improvement of SO₂ diffusion to solid sorbent and optimization of reactor structure.     

Retention mechanism of calcium ferrite and compositions of ash on selenium during chemical looping gasification

Selenium pollution by coal utilization is of increasing concern. Calcium-iron (Ca–Fe) oxygen carriers (OCs) and alkali metal ions have strong inhibitory effects on selenium, which can reduce the emissions of selenium vapor. The retention mechanisms of selenium by Fe₂O₃, CaFe₂O₄, Ca₂Fe₂O₅ and bottom ash are investigated during chemical looping gasification (CLG). Iron-based OC can oxidize H₂Se(g) to SeO₂(g); furthermore, lattice oxygen is released by Fe₂O₃, contributing to the formation of an Fe–O–Se structure to retain selenium and form selenite. Because calcium ferrite is poorly oxidizing, it cannot oxidize H₂Se(g), but the CaO produced when OCs are reduced can react with H₂Se(g) to form CaSe(s), and this process can be promoted by H₂S(g). The best retention rates reached 32.301% when Ca₂Fe₂O₅ was used. In the cyclic experiment, the selenium retention of the bottom ash gradually increases. Alkali metal ions in bottom ash are the main factor in retaining selenium. Ca²⁺ and Mg²⁺ do not easily vaporize due to their high melting points; therefore, their selenium retention is significantly better than that of K⁺ and Na⁺. This research provided a new idea for the removal of selenium by using OCs and bottom ash particles during CLG.