Mechanism and dynamic study of reactive red X-3B dye degradation by ultrasonic-assisted ozone oxidation process

The effectiveness of ozone combined with ultrasound techniques in degrading reactive red X-3B is evaluated. A comparison among ozone (O₃), ultrasonic (US), ozone/ultrasonic (O₃/US) for degradation of reactive red X-3B has been performed. Results show that O₃/US system was the most effective and the optimally synergetic factor reaches to 1.42 in O₃/US system. The cavitation of ultrasound plays an important role during the degradation process. It is found that 99.2% of dye is degraded within 6 min of reaction at the initial concentration of 100 mg·L⁻¹, pH of 6.52, ozone flux of 40 L·h⁻¹ and ultrasonic intensity of 200 W·L⁻¹. Ozonation reactions in conjunction with sonolysis indicate that the decomposition followed pseudo-first-order reaction kinetics but the degradation efficiencies are affected by operating conditions, particularly initial pH and ultrasonic intensity. A kinetic model is established based on the reaction corresponding to operational parameters. In addition, the main reaction intermediates, such as p-benzoquinone, catechol, hydroquinone, phthalic anhydride and phthalic acid, are separated and identified using GC/MS and a possible degradation pathway is proposed during the O₃/US process.     

Application of ZnO nanorods loaded on activated carbon for ultrasonic assisted dyes removal: Experimental design and derivative spectrophotometry method

A method based on application of ZnO nanorods loaded on activated carbon (ZnO-NRs-AC) for adsorption of Bromocresol Green (BCG) and Eosin Y (EY) accelerated by ultrasound was described. The present material was synthesized under ultrasound assisted wet-chemical method and subsequently was characterized by FE-SEM, TEM, BET and XRD analysis. The extent of contribution of conventional variables like pH (2.0–10.0), BCG concentration (4–20 mg L⁻¹), EY concentration (3–23 mg L⁻¹), adsorbent dosage (0.01–0.03 g), sonication time (1–5 min) and centrifuge time (2–6 min) as main and interaction part were investigated by central composite design under response surface methodology. Analysis of variance (ANOVA) was adapted to experimental data and guide the best operational conditions mass by set at 6.0, 9 mg L⁻¹, 10 mg L⁻¹, 0.02 g, 4 and 4 min for pH, BCG concentration, EY concentration, adsorbent dosage, sonication and centrifuge time, respectively. At these specified conditions dye adsorption efficiency was higher than 99.5%. The suitability and well prediction of optimum point was tested by conducting five experiments and respective results revel that RSD% was lower than 3% and high quality of fitting was confirmed by t-test. The experimental data were best fitted in Langmuir isotherm equation and the removal followed pseudo second order kinetics. The experimentally obtained maximum adsorption capacities were estimated as 57.80 and 61.73 mg g⁻¹ of ZnO-NRs-AC for BCG and EY respectively from binary dye solutions. The mechanism of removal was explained by boundary layer diffusion via intraparticle diffusion.     

Hydrogen permeation of tungsten phosphate glass thin films

Thin films of tungsten phosphate glasses were deposited on a Pd substrate by a pulsed laser deposition method and the flux of hydrogen passed thorough the glass film was measured with a conventional gas permeation technique in the temperature range 300–500 °C. The glass film deposited at low oxygen pressure was inappropriate for hydrogen permeation because of reduction of W ions due to oxygen deficiency. The membrane used in the hydrogen permeation experiment was a 3-layered membrane and consisted of Pd film (~ 20 nm), the glass film (≤ 300 nm) and the Pd substrate (250 µm). When the pressure difference of hydrogen and thickness of the glass layer were respectively 0.2 MPa and ~ 100 nm, the permeation rate through the membrane was 2.0 × 10^? 6 mol cm^? 2 s^? 1 at 500 °C. It was confirmed that the protonic and electronic mixed conducting glass thin film show high hydrogen permeation rate.     

Ultrasound-assisted acid hydrolysis of cellulose to chemical building blocks: Application to furfural synthesis

In this work, the use of ultrasound energy for the production of furanic platforms from cellulose was investigated and the synthesis of furfural was demonstrated. Several systems were evaluated, as ultrasound bath, cup horn and probe, in order to investigate microcrystalline cellulose conversion using simply a diluted acid solution and ultrasound. Several acid mixtures were evaluated for hydrolysis, as diluted solutions of HNO₃, H₂SO₄, HCl and H₂C₂O₄. The influence of the following parameters in the ultrasound-assisted acid hydrolysis (UAAH) were studied: sonication temperature (30 to 70 °C) and ultrasound amplitude (30 to 70% for a cup horn system) for 4 to 8 mol L⁻¹ HNO₃ solutions. For each evaluated condition, the products were identified by ultra-performance liquid chromatography with high-resolution time-of-flight mass spectrometry (UPLC-ToF-MS), which provide accurate information regarding the products obtained from biomass conversion. The furfural structure was confirmed by nuclear magnetic resonance (¹H and ¹³C NMR) spectroscopy. In addition, cellulosic residues from hydrolysis reaction were characterized using scanning electron microscopy (SEM), which contributed for a better understanding of physical-chemical effects caused by ultrasound. After process optimization, a 4 mol L⁻¹ HNO₃ solution, sonicated for 60 min at 30 °C in a cup horn system at 50% of amplitude, lead to 78% of conversion to furfural. This mild temperature condition combined to the use of a diluted acid solution represents an important contribution for the selective production of chemical building blocks using ultrasound energy.     

Rapid preparation of high electrochemical performance LiFePO4/C composite cathode material with an ultrasonic-intensified micro-impinging jetting reactor

A joint chemical reactor system referred to as an ultrasonic-intensified micro-impinging jetting reactor (UIJR), which possesses the feature of fast micro-mixing, was proposed and has been employed for rapid preparation of FePO₄ particles that are amalgamated by nanoscale primary crystals. As one of the important precursors for the fabrication of lithium iron phosphate cathode, the properties of FePO₄ nano particles significantly affect the performance of the lithium iron phosphate cathode. Thus, the effects of joint use of impinging stream and ultrasonic irradiation on the formation of mesoporous structure of FePO₄ nano precursor particles and the electrochemical properties of amalgamated LiFePO₄/C have been investigated. Additionally, the effects of the reactant concentration (C = 0.5, 1.0 and 1.5 mol L⁻¹), and volumetric flow rate (V = 17.15, 51.44, and 85.74 mL min⁻¹) on synthesis of FePO₄·2H₂O nucleus have been studied when the impinging jetting reactor (IJR) and UIJR are to operate in nonsubmerged mode. It was affirmed from the experiments that the FePO₄ nano precursor particles prepared using UIJR have well-formed mesoporous structures with the primary crystal size of 44.6 nm, an average pore size of 15.2 nm, and a specific surface area of 134.54 m² g⁻¹ when the reactant concentration and volumetric flow rate are 1.0 mol L⁻¹ and 85.74 mL min⁻¹ respectively. The amalgamated LiFePO₄/C composites can deliver good electrochemical performance with discharge capacities of 156.7 mA h g⁻¹ at 0.1 C, and exhibit 138.0 mA h g⁻¹ after 100 cycles at 0.5 C, which is 95.3% of the initial discharge capacity.     

Mixed oxygen ion and electron conducting hollow fiber membranes for oxygen separation

Phase inversion spinning technique was employed to prepare dense perovskite hollow fiber membranes made from composition BaCo_xFe_yZr_zO_3−δ (BCFZ, x + y + z = 1.0). Scanning electron microscope (SEM) shows that such hollow fibers have an asymmetric structure, which is favored to the oxygen permeation. An oxygen permeation flux of 7.6 cm³/min cm² at 900 °C under an oxygen gradient of 0.209 × 10⁵ Pa/0.065 × 10⁵ Pa was achieved. From the Wagner Theory, the oxygen permeation through the hollow fiber membrane is controlled by both bulk diffusion and surface exchange. The elements composition of fresh fiber and the fiber after long-term experiments were analyzed by energy-dispersive X-ray spectra (EDXS). Compared to the fresh fiber, sulphur was found on the tested hollow fiber membrane surface exposed to the air side and in the bulk, and Ba segregations occur on the tested hollow fiber membrane surface exposed to the air side. A decrease of the oxygen permeation flux was observed, which was probably due to the sulphur poisoning.     

Mixed conductivity and oxygen permeability of doped Pr2NiO4-based oxide

Pr₂NiO₄-based oxide was studied as a new mixed electronic and oxide ionic conductor for the oxygen permeation membrane. It was found that Pr₂NiO₄ doped with Cu and Fe for Ni site exhibits the relatively high oxygen permeation rate. Doping second cation to Ni site is effective for improving the oxygen permeation rate and the trivalent cation seems to be effective for increasing the oxygen permeation rate. Among the examined cation, the highest oxygen permeation rate was obtained by doping 5 mol% Fe. The oxygen permeation rate was also significantly affected by the surface catalyst and the highest oxygen permeation rate of 80 μmol·min^− 1·cm^− 2 at 1273 K was achieved by using La_0.1Sr_0.9Co_0.9Fe_0.1O₃ for the surface catalyst. Since the electrical conductivity slightly decreased with decreasing P_O2 and it dropped significantly at P_O2 = 10^− 19 atm, chemical stability of Pr₂NiO₄-based oxide seems to be reasonably high. Application of this new mixed conductor for the oxygen permeation membrane under the CH₄ partial oxidation was also studied and it was confirmed that the oxygen permeation rate much improved under the CH₄ oxidation condition and this Pr₂NiO₄ can be used for the oxygen permeation membrane for the CH₄ partial oxidation.     

Conductivity and oxygen permeability of a novel oxide Pr2Ni0.8 − x Cu0.2FexO4 and its application to partial oxidation of CH4

Iron-doped Pr₂Ni_0.8Cu_0.2O₄ was studied as a new mixed electronic and oxide-ionic conductor for use as an oxygen-permeating membrane. An X-ray diffraction analysis suggested that a single phase K₂NiF₄-type structure was obtained in the composition range from x = 0 to 0.05 in Pr₂Ni_0.8 − xCu_0.2Fe_xO₄. It is considered that the doped Fe is partially substituted at the Ni position in Pr₂NiO₄. The prepared Pr₂NiO₄-based oxide exhibited a dominant hole conduction in the P_O2 range from 1 to 10^− 21 atm. The electrical conductivity of Pr₂Ni_0.8−xCu_0.2Fe_xO₄ is as high as 10² S cm^− 1 in the temperature range of 873–1223 K and it gradually decreased with the increasing amount of Fe substituted for Ni. The oxygen permeation rate was significantly enhanced by the Fe doping and it was found that the highest oxygen permeation rate (60 μmol min^− 1 cm^− 2) from air to He was achieved for x = 0.05 in Pr₂Ni_0.8 − xCu_0.2Fe_xO₄. Since the chemical stability of the Pr₂NiO₄-based oxide is high, Pr₂Ni_0.75Cu_0.2Fe_0.05O₄ can be used as the oxygen-separating membrane for the partial oxidation of CH₄. It was observed that the oxygen permeation rate was significantly improved by changing from He to CH₄ and the observed permeation rate reached a value of 225 μmol min^− 1 cm^− 2 at 1273 K for the CH₄ partial oxidation.     

Organic light sources look forward to optimize the photosynthesis process

We introduce a series of organic LEDs that exploit the monomer and excimer emissions from single phosphor dopant emitters. These organic LEDs were found to be effective in the simultaneous creation of blue and red emission bands essential for plant growth. By varying the concentration of novel phosphorescent dopants selected from a series of newly synthesized platinum complexes [PtL^22–25Cl], we have manufactured the blue-biased LEDs [with the Commission Internationale de L’Eclairage (CIE) coordinates (x, y) (0.27, 0.37)] and the red-biased LEDs [CIE coordinates (0.53, 0.38)], at a high luminance of ≈500 cd/m² and with external electroluminescence (EL) quantum efficiency of 15–18% photon/electron (→ power efficiency 8–12 lm/W). The EL spectrum most suitable for the action spectrum of photosynthesis yield was that of a device incorporating 20 wt.% content of [PtL²³Cl]. This LED yielded photosynthetic photon flux (PPF) approaching 10 μmol s⁻¹ W⁻¹ of the electrical power, a value which significantly exceeds that for the professional lamps used commonly for horticultural lighting.     

Extraction mechanism of ultrasound assisted extraction and its effect on higher yielding and purity of artemisinin crystals from Artemisia annua L. leaves

This study proposes an ultrasound-horn system for the extraction of a natural active compound “artemisinin” from Artemisia annua L. leaves as an alternative to hot maceration technique. Ultrasound leaching improves artemisinin recovery at all temperatures where only ten minutes is required to recover 70% (4.42 mg g⁻¹) compared to 60 min of conventional hot leaching for the same yield. For instance, ultrasound treatment at 30 °C produced a higher yield than the one obtained by conventional maceration at 40 °C. Kinetic study suggests that the extraction pattern can be assimilated, during the first ten minutes, to a first order steady state, from which activation energy calculations revealed that each gram of artemisinin required 7.38 kJ in ultrasound versus 10.3 kJ in the conventional system. Modeling results indicate the presence of two extraction stages, a faster stage with a diffusion coefficient of 19 × 10⁻⁵ cm² min⁻¹ for ultrasound technique at 40 °C, seven times higher than the conventional one; and a second deceleration stage similar for both techniques with diffusion coefficient ranging from 1.7 to 3.1 × 10⁻⁵ cm² min⁻¹. It is noted that the efficient ultrasound extraction potential implies extraction of higher amount of co-metabolites so low artemisinin crystal purity is engendered but a combination with a purification step using activated charcoal and celite adsorbents produced crystals with comparable purity for conventional and ultrasound samples.     

Ultrasonic assisted-Fenton-like degradation of nitrobenzene at neutral pH using nanosized oxides of Fe and Cu

Ultrasonic-assisted heterogeneous Fenton reaction was used for degradation of nitrobenzene (NB) at neutral pH conditions. Nano-sized oxides of α-Fe₂O₃ and CuO were prepared, characterized and tested in degradation of NB (10 mg L⁻¹) under sonication of 20 kHz at 25 °C. Complete degradation of NB was effected at pH 7 in presence of 10 mM H₂O₂ after 10 min of sonication in presence of α-Fe₂O₃ (1.0 g L⁻¹), (k = 0.58 min⁻¹) and after 25 min in case of CuO (k = 0.126 min⁻¹). α-Fe₂O₃ showed also effective degradation under the conditions of 0.1 g L⁻¹ oxide and 5.0 mM of H₂O₂, even though with a lower rate constant (0.346 min⁻¹). Sonication plays a major role in enhancing the production of hydroxyl radicals in presence of solid oxides. Hydroxyl radicals-degradation pathway is suggested and adopted to explain the differences noted in rate constants recorded on using different oxides.     

Oxygen permeability and stability of Ba0.5Sr0.5Co0.8Fe0.2O3−δ as an oxygen-permeable membrane at high pressures

Oxygen permeation fluxes across the dense Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3−δ (BSCFO) membrane disks were measured under an air/helium oxygen partial pressure gradient at high pressures (up to 10 atm) and various temperatures (973–1123 K). The fabricated BSCFO membrane exhibited good oxygen permeability with a high oxygen permeation flux of 2.01 ml min^− 1cm^− 2 (thickness: 1.37 mm) at 1123 K and 10 atm. Oxygen permeation results were analyzed theoretically using the surface exchange current model. The dependences of the oxygen permeation fluxes on the oxygen partial pressure gradient, suggested that the bulk oxygen ionic diffusion was the rate-limiting step for the overall oxygen permeation process across the BSCFO membrane. The ambipolar diffusion coefficients (D_a), the oxygen vacancy diffusion coefficients (D_v) and the oxygen ionic conductivities (σ_i) of the BSCFO material at different temperatures (973–1123 K) were calculated. It was found that BSCFO possessed high oxygen diffusion coefficients and ionic conductivities, which resulted in the good oxygen permeability of BSCFO. In addition, the BSCFO membrane exhibited good stability of oxygen permeation at 1123 K, while the deterioration of oxygen permeation stability was observed at 1098 K due to structural changes occurring at the surface of the BSCFO membrane disk as demonstrated by XRD.     

Chloroethene dehalogenation with ultrasonically produced air-stable nano iron

Zerovalent iron (ZVI) has been demonstrated to be suitable for the dehalogenation of environmental pollutants such as chloroethenes. The construction of ZVI reactive barriers by conventional engineering measures is expensive and limited to shallow aquifers. The use of nanosized ZVI particles opens new opportunities to construct ZVI barriers with less invasive techniques. However, nanosized particles of pure ZVI are pyrophoric and react spontaneously with atmospheric oxygen.In this study, nanosized air-stable ZVI particles were produced by applying ultrasound to a solution of Fe(CO)₅ in edible oil. The resulting iron nanoparticles were dispersed in a carbon matrix, and coated with a non-crystalline carbon layer of approx. 2.5 nm. Although, these nanoparticles are non-pyrophoric and stable in air, dechlorination of tetrachloroethene was demonstrated in synthetic aqueous medium and in polluted groundwater. Additionally, hydrogen was formed. Due to the larger surface area, significantly higher mass-normalized reaction rates of the novel carbon-coated nanoparticles were obtained as compared to conventional bulk ZVI material. Surface normalized pseudo-first-order-reaction rates of k_SA = 3.49 × 10^?3 L h^?1 m^?2 and 2.33 × 10^?2 L h^?1 m^?2 were calculated for the nano-ZVI and the bulk ZVI, respectively. Dechlorination reaction products of the novel nano-ZVI were trichloroethene, cis-dichloroethene, vinyl chloride, ethene, and ethane.     

Study and optimization of the ultrasound-enhanced cleaning of an ultrafiltration ceramic membrane through a combined experimental–statistical approach

Membrane fouling is one of the main drawbacks of ultrafiltration technology during the treatment of dye-containing effluents. Therefore, the optimization of the membrane cleaning procedure is essential to improve the overall efficiency. In this work, a study of the factors affecting the ultrasound-assisted cleaning of an ultrafiltration ceramic membrane fouled by dye particles was carried out. The effect of transmembrane pressure (0.5, 1.5, 2.5 bar), cross-flow velocity (1, 2, 3 m s⁻¹), ultrasound power level (40%, 70%, 100%) and ultrasound frequency mode (37, 80 kHz and mixed wave) on the cleaning efficiency was evaluated. The lowest frequency showed better results, although the best cleaning performance was obtained using the mixed wave mode.A Box–Behnken Design was used to find the optimal conditions for the cleaning procedure through a response surface study. The optimal operating conditions leading to the maximum cleaning efficiency predicted (32.19%) were found to be 1.1 bar, 3 m s⁻¹ and 100% of power level.Finally, the optimized response was compared to the efficiency of a chemical cleaning with NaOH solution, with and without the use of ultrasound. By using NaOH, cleaning efficiency nearly triples, and it improves up to 25% by adding ultrasound.     

Molybdenum carbide nano-sheet as a high capacity anode material for monovalent alkali metal-ion batteries—Theoretical investigation

This contribution presents a theoretical investigation of monovalent metal-ion adsorption and diffusion on two-dimensional (2D) buckled nanostructure of molybdenum carbide (MoC) by using the first principle method. We find that buckled MoC nanostructure exhibits great stability, semiconducting electronic property, and high performance as electrode material. Interestingly, Crystal Orbital Hamilton population (COHP) method results show that buckled MoC is chemically stable in a wide range of temperatures, and various Li, Na, ions adsorbed configurations, which is beneficial for anode materials. Especially, single-layer MoC exhibits a superior theoretical capacity of 993.16 mA h g⁻¹ for Li-ions and 496.58 mA h g⁻¹ for Na/K-ions. The storage capacity of 1200 mA h g⁻¹ is found for the adsorption of ions on multilayer bulk MoC. Moreover, migration energy barriers are predicted as 0.38 eV for Li, 0.32 eV for Na, and 0.24 eV for K; these remarkable results determine the applicability of buckled MoC as ideal anode material for metal-ion battery applications.     

Sonoelectrochemical degradation of triclosan in water

The sonoelectrochemical degradation of triclosan in aqueous solutions with high-frequency ultrasound (850 kHz) and various electrodes was investigated. Diamond coated niobium electrode showed the best results and was used as standard electrode, leading to effective degradation and positive synergistic effect. The influence of different parameters on the degradation degree and energy efficiency were evaluated and favorable reaction conditions were found. It could be shown that 92% of triclosan (1 mg L⁻¹ aqueous solution) was degraded within 15 min, following pseudo-first order kinetics.     

Sonocatalyzed decolorization of synthetic textile wastewater using sonochemically synthesized MgO nanostructures

The present study focused on the synthesis of nanostructured MgO via sonochemical method and its application as sonocatalyst for the decolorization of Basic Red 46 (BR46) dye under ultrasonic irradiation. The sonocatalyst was characterized using X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM) equipped with energy dispersive X-ray microanalysis (EDX). In the following, the sonocatalytic removal of the dye under different operational conditions was evaluated kinetically on the basis of pseudo first-order kinetic model. The reaction rate of sonocatalyzed decolorization using MgO nanostructures (12.7 × 10⁻³ min⁻¹) was more efficient than that of ultrasound alone (2.0 × 10⁻³ min⁻¹). The increased sonocatalyst dosage showed better sonocatalytic activity but the application of excessive dosage should be avoided. The presence of periodate ions substantially increased the decolorization rate from 14.76 × 10⁻³ to 33.4 × 10⁻³ min⁻¹. Although the application of aeration favored the decolorization rate (17.8 × 10⁻³ min⁻¹), the addition of hydrogen peroxide resulted in a considerable decrease in the decolorization rate (9.5 × 10⁻³ min⁻¹) due to its scavenging effects at specific concentrations. Unlike alcoholic compounds, the addition of phenol had an insignificant scavenging effect on the sonocatalysis. A mineralization rate of 7.4 × 10⁻³ min⁻¹ was obtained within 120 min. The intermediate byproducts were also detected using GC–MS analysis.     

Trace determination of safranin O dye using ultrasound assisted dispersive solid-phase micro extraction: Artificial neural network-genetic algorithm and response surface methodology

In this study, ultrasound assisted dispersive solid-phase micro extraction combined with spectrophotometry (USA-DSPME-UV) method based on activated carbon modified with Fe₂O₃ nanoparticles (Fe₂O₃-NPs-AC) was developed for pre-concentration and determination of safranin O (SO). It is known that the efficiency of USA-DSPME-UV method may be affected by pH, amount of adsorbent, ultrasound time and eluent volume and the extent and magnitude of their contribution on response (in term of main and interaction part) was studied by using central composite design (CCD) and artificial neural network-genetic algorithms (ANN-GA). Accordingly by adjustment of experimental conditions suggested by ANN-GA at pH 6.5, 1.1 mg of adsorbent, 10 min ultrasound and 150 μL of eluent volume led to achievement of best operation performance like low LOD (6.3 ng mL⁻¹) and LOQ (17.5 ng mL⁻¹) in the range of 25–3500 ng mL⁻¹. In following stage, the SO content in real water and wastewater samples with recoveries between 93.27–99.41% with RSD lower than 3% was successfully determined.     

Thermosonication as a potential quality enhancement technique of apple juice

Enzymatic browning and microbial growth lead to quality losses in apple products. In the present study, fresh apple juice was thermosonicated using ultrasound in-bath (25 kHz, 30 min, 0.06 W cm⁻³) and ultrasound with-probe sonicator (20 kHz, 5 and 10 min, 0.30 W cm⁻³) at 20, 40 and 60 °C for inactivation of enzymes (polyphenolase, peroxidase and pectinmethylesterase) and microflora (total plate count, yeast and mold). Additionally, ascorbic acid, total phenolics, flavonoids, flavonols, pH, titratable acidity, ^°Brix and color values influenced by thermosonication were investigated. The highest inactivation of enzymes was obtained in ultrasound with-probe at 60 °C for 10 min, and the microbial population was completely inactivated at 60 °C. The retention of ascorbic acid, total phenolics, flavonoids and flavonols were significantly higher in ultrasound with-probe than ultrasound in-bath at 60 °C. These results indicated the usefulness of thermosonication for apple juice processing at low temperature, for enhanced inactivation of enzymes and microorganisms.     

Oxygen permeation characteristics of zirconia with surface modification

Yttria-stabilized zirconia (YSZ) can be used as an oxygen-permeating membrane at elevated temperature (> 1400 °C) due to its chemical and mechanical stability. It was previously shown that the oxygen transport through YSZ membrane in reducing oxygen partial pressure (P_O2) was highly influenced by the surface-exchange kinetics that can be improved by porous surface coating layers such as YSZ, GDC (Gd-doped ceria) or YSZ–GDC mixture [H.J. Park, G.M. Choi, J. Eur. Ceram. Soc. 25 (2005) 2577]. However, the increased oxygen flux was still lower than that estimated assuming bulk-diffusion limit and rapidly decreased with time due to the sintering of coating layers and the reaction between bulk YSZ and coating layers. In this study, the oxygen fluxes through YSZ with LaCrO₃, GDC + LaCrO₃ (bilayer), LaCrO₃ + 5 wt.% GDC (mixture), or LaCr_0.7Co_0.3O₃ coatings were measured under controlled P_O2 gradient (permeate-side P_O2: ∼ 3 × 10^− 12 atm, feed-side P_O2: 2 × 10^− 10–2 × 10^− 8 atm) at 1600 °C. The oxygen flux drastically increased with these coatings. The highest increase in oxygen flux was shown with GDC + LaCrO₃ (bilayer) coating and was maintained for a long time. The presence of highly catalytic Ce ions while maintaining porous structure in the coating layer may explain the observation. The prevention of formation of resistive layer due to ceria coating may also be partly responsible for the observation.