Preparation and anti-oxidation performance of Al2O3-containing TaSi2–MoSi2–borosilicate glass coating on porous SiCO ceramic composites for thermal protection

In order to improve the thermal oxidation resistance of carbon fiber-reinforced porous silicon oxycarbide (SiCO) ceramic composites, an Al₂O₃-containing TaSi₂–MoSi₂–borosilicate glass coating was formed on the surface of the composites via brushing and sintering. The anti-oxidation property of the coated composites at 1873 K was investigated. Microstructures and chemical compositions of the sample before and after anti-oxidation test were determined using XRD, SEM and EDS. After heating in air at 1873 K for 20 min, the Al₂O₃-containing TaSi₂–MoSi₂–borosilicate glass coating effectively protects the SiCO ceramic composites and the coated sample kept its appearance well without obvious defects on the surface. The cross-sectional SEM images show that the coating is covered by a film of oxidation products with a thickness of about 40 μm, which is dense and crack free. Inside the A-TMG coating, irregular-shaped silicides are surrounded by continuous borosilicate glass and no penetrating holes or visible cracks are found. Al₂O₃ increases the viscosity of the borosilicate glass, which improves oxidation resistance of the coated sample by enhancing gas-penetration resistance of the glass. In contrast, the sample without Al₂O₃ in the coating slurry is severely oxidized and exhibits lots of open pores on the surface after oxidation test.

Al₂O₃ improves the oxidation resistance of TaSi₂–MoSi₂–borosilicate glass coating through increasing the viscosity and inhibiting gas penetration into matrix at high temperature, thus prevents porous SiCO ceramic composites from being oxidized.     

Microstructure,friction and corrosion resistance properties of a Ni–Co–Al2O3 composite coating

Ni–Co–Al₂O₃ composite coatings were prepared by pulsed electrodeposition and electrophoresis–electrodeposition on aluminum alloy. The content of Al₂O₃ particles of the Ni–Co–Al₂O₃ composite coating prepared by electrophoresis–electrodeposition was significantly higher than the composite coating prepared by pulsed electrodeposition. The composite coating prepared by electrophoresis–electrodeposition exhibited a better anti-wear performance than that prepared by pulsed electrodeposition. The morphology, composition and microstructure of the composite coatings were determined by means of X-ray diffractometer (XRD) and scanning electron microscopy (SEM). The hardness and friction properties of the samples were tested on the microhardness tester and the friction and wear loss tester respectively.

Ni–Co–Al₂O₃ composite coatings were prepared by pulsed electrodeposition and electrophoresis–electrodeposition on aluminum alloy.     

Reactive adsorption desulfurization of NiO and Ni0 over NiO/ZnO–Al2O3–SiO2 adsorbents: role of hydrogen pretreatment

Reactive adsorption desulfurization (RADS) of Fluidized Catalytically Cracked (FCC) gasoline on reduced and unreduced NiO/ZnO–Al₂O₃–SiO₂ adsorbents was studied. Various characterizations such as powder X-ray diffraction (XRD), H₂-temperature-programmed reduction (H₂-TPR), the H₂/O₂ pulse titration (HOPT), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) are used to evaluate the effects of hydrogen pretreatment of the adsorbents. XRD and HOPT results indicate that NiO is hard to be reduced to Ni⁰ under the conditions of RADS. H₂-TPR shows that NiO might be reduced to Ni⁰ at the temperature of 598 °C, much higher than the temperature of RADS. The Ni 2p_3/2 spectrum of Ni⁰ is not observed for the reduced adsorbent, but the main peak of Ni 2p_3/2 of NiS is found for the spent adsorbent. The unreduced NiO/ZnO–Al₂O₃–SiO₂ adsorbent performs a better desulfurization than the reduced adsorbent at the beginning of desulfurization process. NiO and Ni⁰ are assumed as the main active components and present a good desulfurization ability in RADS. Finally, a change in the RADS mechanism is presented and discussed.

A possible reaction mechanism of desulfurization on NiO/ZnO–Al₂O₃–SiO₂ is discussed.     

Effect of unmelted lime on the element distribution behavior on a CaO–SiO2–MgO–Al2O3–FeO–CaF2(–Cr2O3) slag

In this study, a CaO–SiO₂–Al₂O₃–MgO–FeO–CaF₂(–Cr₂O₃) slag was chosen according to the compositions of the stainless steel slag for industrial production, and a CaO block was added to the molten slag after the synthetic slag was fully melted. The influences of unmelted lime on the distribution of elements and the structure of product layers at the lime/slag boundary, particularly the existing state of chromium oxide in the chromium-bearing stainless steel slag, were deeply discussed by scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) and FactSage 7.1. The experiment results indicated that when the unmelted lime existed in the CaO–SiO₂–Al₂O₃–MgO–FeO–CaF₂ slag system, two product layers of periclase (MgO) and dicalcium silicate (Ca₂SiO₄) at the boundary of the CaO block were formed. However, when the CaO block was added in the CaO–SiO₂–Al₂O₃–MgO–FeO–CaF₂–Cr₂O₃ stainless steel slag, besides MgO and Ca₂SiO₄ product layers, needle-shaped calcium chromite (CaCr₂O₄) was also precipitated around the CaO block. Moreover, a small amount of Cr dissolved in the periclase phase. Eh–pH diagrams showed that the CaCr₂O₄ and MgO phase unstably existed in a weak acid aqueous solution. Therefore, the existence of unmelted lime in the stainless steel slag could enhance the leachability of chromium.

The effect of unmelted lime on the distribution of elements and structure of product layers in CaO–SiO₂–MgO–Al₂O₃–FeO–CaF₂(–Cr₂O₂) stainless steel slag and the action of unmelted lime phase mechanism in experimental slags was conducted.     

A modified random network model for P2O5–Na2O–Al2O3–SiO2 glass studied by molecular dynamics simulations

We investigated the short- and medium-range structural features of sodium aluminosilicate glasses with various P₂O₅ (0–7 mol%) content and Al/Na ratios ranging from 0.667 to 2.000 by using molecular dynamics simulations. The local environment evolution of network former cations (Si, Al, P) and the extent of clustering behavior of modifiers (Na⁺) is determined through pair distribution function (PDF), total correlation function (TDF), coordination number (CN), Q_xⁿ distribution and oxygen speciation analysis. We show that Al–O–P and Si–O–Al linkage is preferred over other connections as compared to a random model and that Si–O–Si linkage is promoted by the P₂O₅ addition, which is related to structural heterogeneity and generates well-separated silicon-rich and aluminum–phosphorus-rich regions. Meanwhile, due to the relatively high propensity of Al to both Si and P, heterogeneity can be partly overcome with high Al content. A small amount of Si–O–P linkages have been detected at the interface of separated regions. Clustering of Na⁺ is also observed and intensified with the addition of P₂O₅. Based on the simulated structural information, a modified random network model for P₂O₅-bearing sodium aluminosilicate glass has been proposed, which could be useful to optimize the mobility of sodium ions and design novel functional glass compositions.

(A) A modified structural model proposed for P₂O₅-bearing sodium aluminosilicate glasses. (B) Degree of preferred connection (DPC) of different T–O–T network linkage for LAP, MAP and HAP glass compositions with various P₂O₅ content.     

The preparation,microstructure and mechanical properties of a dense MgO–Al2O3–SiO2 based glass-ceramic coating on porous BN/Si2N2O ceramics

A dense MgO–Al₂O₃–SiO₂ based glass-ceramic coating was prepared by a doctor blade process on a porous BN/Si₂N₂O ceramic surface followed by heat treatment at 1050 °C under nitrogen flow. The phase composition, microstructure, mechanical properties and water absorption of the coating were studied. The coating consisted of α-cordierite phase with a small amount of glass phase. The dense coating without pores and cracks was favorable to seal and densify the porous ceramic surface due to part of the molten glass infiltrating the surface pores. The coating was defect-free and tightly bonded to the substrate because of a larger bonding area between the coating and the substrate. The elastic modulus and bending strength of the glass-ceramic coating were 37.9 GPa and 67.1 MPa, respectively. Moreover, the coated samples had a high Vickers hardness and low water absorption.

A dense MgO–Al₂O₃–SiO₂ based glass-ceramic coating was prepared by a doctor blade process on a porous BN/Si₂N₂O ceramic surface followed by heat treatment at 1050 °C under nitrogen flow.     

Preparation and heat-insulating properties of Al2O3–ZrO2(Y2O3) hollow fibers derived from cogon using an orthogonal experimental design

Bionic design is efficient to develop high-performance lightweight refractories with sophisticated structures such as hollow ceramic fibers. Here, we report a four-stage procedure for the preparation of Al₂O₃–ZrO₂(Y₂O₃) hollow fibers using the template of cogon—a natural grass. Subsequently, to optimize the thermal performance of the fibers, four sets of preparation parameters, namely, x(Al₂O₃), solute mass ratio of the mixture, dry temperature, and sintering temperature were investigated. Through an orthogonal design, the optimal condition of each parameter was obtained as follows: x(Al₂O₃) was 0.70, solute mass ratio of the mixture was 15 wt%, dry temperature was 80 °C, and sintering temperature was 1100 °C. Overall, Al₂O₃–ZrO₂(Y₂O₃) hollow fibers show relatively low thermal conductivity (0.1038 W m⁻¹ K⁻¹ at 1000 °C), high porosity (95.0%), and low density (0.05–0.10 g cm⁻³). The multiphase compositions and morphology of Al₂O₃–ZrO₂(Y₂O₃) hollow fibers, which may contribute to their thermal properties, were also discussed.

Lightweight Al₂O₃–ZrO₂(Y₂O₃) hollow fibers with low thermal conductivity were prepared by a natural template—cogon grass.     

The influence of composition on the functionality of hybrid CuO–ZnO–Al2O3/HZSM-5 for the synthesis of DME from CO2 hydrogenation

A series of CuO–ZnO–Al₂O₃/HZSM-5 hybrid catalysts with different Cu/Zn ratios and disparate Al₂O₃ doping were prepared and characterized by XRD, BET, H₂-TPR, NH₃-TPD and XPS techniques. The optimal Cu/Zn ratio is 7 : 3, and the introduction of a suitable amount of Al₂O₃ to form hybrid catalysts increased the BET specific area and micropore volume, facilitated the CuO dispersion, decreased the CuO crystallite size, increased the interaction between CuO and ZnO, enhanced the number of weak acid sites, altered the copper chemical state and improved the catalytic performance consequently. The highest CO₂ conversion, DME selectivity and DME yield of 27.3%, 67.1% and 18.3%, respectively, were observed over the CZA₇H catalyst. The suitable temperature of 260 °C and the appropriate space velocity of 1500 h⁻¹ for one-step synthesis of dimethyl ether (DME) from carbon dioxide (CO₂) hydrogenation were also investigated. The 50 h stability of the CZA₇H catalyst was also tested.

The introduction of Al₂O₃ increased the number of weak acid sites, altered the copper chemical state and improved the catalytic performance and stability consequently.     

Continuous selective deoxygenation of palm oil for renewable diesel production over Ni catalysts supported on Al2O3 and La2O3–Al2O3

The present study provides, for the first time in the literature, a comparative assessment of the catalytic performance of Ni catalysts supported on γ-Al₂O₃ and γ-Al₂O₃ modified with La₂O₃, in a continuous flow trickle bed reactor, for the selective deoxygenation of palm oil. The catalysts were prepared via the wet impregnation method and were characterized, after calcination and/or reduction, by N₂ adsorption/desorption, XRD, NH₃-TPD, CO₂-TPD, H₂-TPR, H₂-TPD, XPS and TEM, and after the time-on-stream tests, by TGA, TPO, Raman and TEM. Catalytic experiments were performed between 300–400 °C, at a constant pressure (30 bar) and different LHSV (1.2–3.6 h⁻¹). The results show that the incorporation of La₂O₃ in the Al₂O₃ support increased the Ni surface atomic concentration (XPS), affected the nature and abundance of surface basicity (CO₂-TPD), and despite leading to a drop in surface acidity (NH₃-TPD), the Ni/LaAl catalyst presented a larger population of medium-strength acid sites. These characteristics helped promote the SDO process and prevented extended cracking and the formation of coke. Thus, higher triglyceride conversions and n-C₁₅ to n-C₁₈ hydrocarbon yields were achieved with the Ni/LaAl at lower reaction temperatures. Moreover, the Ni/LaAl catalyst was considerably more stable during 20 h of time-on-stream. Examination of the spent catalysts revealed that both carbon deposition and degree of graphitization of the surface coke, as well as, the extent of sintering were lower on the Ni/LaAl catalyst, explaining its excellent performance during time-on-stream.

Highly selective and stable Ni supported on La₂O₃–Al₂O₃ catalyst on the deCO/deCO₂ reaction paths for the production of renewable diesel.     

Large area Al2O3–Au raspberry-like nanoclusters from iterative block-copolymer self-assembly

In the field of functional nanomaterials, core–satellite nanoclusters have recently elicited great interest due to their unique optoelectronic properties. However, core–satellite synthetic routes to date are hampered by delicate and multistep reaction conditions and no practical method has been reported for the ordering of these structures onto a surface monolayer. Herein we show a reproducible and simplified thin film process to fabricate bimetallic raspberry nanoclusters using block copolymer (BCP) lithography. The fabricated inorganic raspberry nanoclusters consisted of a ∼36 nm alumina core decorated with ∼15 nm Au satellites after infusing multilayer BCP nanopatterns. A series of cylindrical BCPs with different molecular weights allowed us to dial in specific nanodot periodicities (from 30 to 80 nm). Highly ordered BCP nanopatterns were then selectively infiltrated with alumina and Au species to develop multi-level bimetallic raspberry features. Microscopy and X-ray reflectivity analysis were used at each fabrication step to gain further mechanistic insights and understand the infiltration process. Furthermore, grazing-incidence small-angle X-ray scattering studies of infiltrated films confirmed the excellent order and vertical orientation over wafer scale areas of Al₂O₃/Au raspberry nanoclusters. We believe our work demonstrates a robust strategy towards designing hybrid nanoclusters since BCP blocks can be infiltrated with various low cost salt-based precursors. The highly controlled nanocluster strategy disclosed here could have wide ranging uses, in particular for metasurface and optical based sensor applications.

Large area Al₂O₃–Au raspberry-like nanoclusters and other complex structures have been created by iterative block-copolymer self-assembly, paving the way to a new generation of on-demand metallic architectures.     

Construction and photocatalytic performance of fluorinated ZnO–TiO2 heterostructure composites

Titanium dioxide, as a promising photocatalytic material, has attracted extensive attention in the field of photocatalytic degradation of organic pollutants in sewage. However, the photocatalytic performance needs to be further improved. In this work, fluorinated ZnO–TiO₂ composites (F-ZTO) were prepared by a simple coprecipitation method. The photocatalytic performance of the samples was studied in detail with methyl orange as the target degradation product. The results indicated that under the same conditions, the degradation rates of 6% F-ZTO, F-TiO₂ and TiO₂ for methyl orange reached 93.75%, 76.56% and 62.89% respectively. This showed that the method used in this work could effectively improve the photocatalytic degradation performance of titanium dioxide. 6% F-ZTO showed an excellent photocatalytic activity, which was attributed to the small grain size, the large specific surface area and the effective inhibition of photoelectron–hole recombination due to fluorination and zinc oxide coupling. In three consecutive cycles, the photocatalytic activity was almost maintained, indicating that 6% F-ZTO had a good recycling performance.

Fluorinated ZnO-TiO₂ composites (F-ZTO) were prepared by a simple coprecipitation method, the method used could effectively improve the photocatalytic property of titanium dioxide, and 6% F-ZTO showed an excellent activity and recycling performance.     

Improvement of low-temperature NH3-SCR catalytic performance over nitrogen-doped MOx–Cr2O3–La2O3/TiO2–N (M = Cu,Fe, Ce) catalysts

A series of MO_x–Cr₂O₃–La₂O₃/TiO₂–N (M = Cu, Fe, Ce) catalysts with nitrogen doping were prepared via the impregnation method. Comparing the low-temperature NH₃-SCR activity of the catalysts, CeCrLa/Ti–N (xCeO₂–yCr₂O₃–zLa₂O₃/TiO₂–N) exhibited the best catalytic performance (NO conversion approaching 100% at 220–460 °C). The physico-chemical properties of the catalysts were characterized by XRD, BET, SEM, XPS, H₂-TPR, NH₃-TPD and in situ DRIFTS. From the XRD and SEM results, N doping affects the crystalline growth of anatase TiO₂ and MO_x (M = Cu, Fe, Ce, Cr, La) which were well dispersed over the support. Moreover, the doping of N promotes the increase of the Cr⁶⁺/Cr ratio and Ce³⁺/Ce ratio, and the surface chemical adsorption oxygen content, which suggested the improvement of the redox properties of the catalyst. And the surface acid content of the catalyst increased with the doping of N, which is related to CeCrLa/TiO₂–N having the best catalytic activity at high temperature. Therefore, the CeCrLa/TiO₂–N catalyst exhibited the best NH₃-SCR performance and the redox performance of the catalysts is the main factor affecting their activity. Furthermore, in situ DRIFTS analysis indicates that Lewis-acid sites are the main adsorption sites for ammonia onto CeCrLa/TiO₂–N and the catalyst mainly follows the L–H mechanism.

A series of MO_x–Cr₂O₃–La₂O₃/TiO₂–N (M = Cu, Fe, Ce) catalysts with nitrogen doping were prepared via the impregnation method.     

Novel mesoporous Co3O4–Sb2O3–SnO2 active material in high-performance capacitive deionization

Capacitive deionization (CDI), as an emerging eco-friendly electrochemical brackish water deionization technology, has widely benefited from carbon/metal oxide composite electrodes. However, this technique still requires further development of the electrode materials to tackle the ion removal capacity/rate issues. In the present work, we introduce a novel active carbon (AC)/Co₃O₄–Sb₂O₃–SnO₂ active material for hybrid electrode capacitive deionization (HECDI) systems. The structure and morphology of the developed electrodes were determined using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and Brunauer–Emmett–Teller (BET)/Barrett–Joyner–Halenda (BJH) techniques, as well as Fourier-transform infrared (FT-IR) spectroscopy. The electrochemical properties were also investigated by cyclic voltammetry (CV) and impedance spectroscopy (EIS). The CDI active materials AC/Co₃O₄ and AC/Co₃O₄–Sb₂O₃–SnO₂ showed a high specific capacity of 96 and 124 F g⁻¹ at the scan rate of 10 mV s⁻¹, respectively. In addition, the newly-developed electrode AC/Co₃O₄–Sb₂O₃–SnO₂ showed high capacity retention of 97.2% after 2000 cycles at 100 mV s⁻¹. Moreover, the electrode displayed excellent CDI performance with an ion removal capacity of 52 mg g⁻¹ at the applied voltage of 1.6 V and in a solution of potable water with initial electrical conductivity of 950 μs cm⁻¹. The electrode displayed a high ion removal rate of 7.1 mg g⁻¹ min⁻¹ with an excellent desalination–regeneration capability while retaining about 99.5% of its ion removal capacity even after 100 CDI cycles.

Capacitive deionization (CDI), as an emerging eco-friendly electrochemical brackish water deionization technology, has widely benefited from carbon/metal oxide composite electrodes.     

Conversion of levulinic acid to γ-valerolactone over Ru/Al2O3–TiO2 catalyst under mild conditions

Novel catalytic material with high catalytic activity and hydrothermal stability plays a key role in the efficient conversion of levulinic acid (LA) to γ-valerolactone (GVL) in water. In this study, mixed oxides Al₂O₃–TiO₂, Al₂O₃–MoO₃ and Al₂O₃–Co₃O₄ were synthesized by co-precipitation using aqueous solution of NaOH as precipitant. Ru catalysts supported on mixed oxides were prepared by impregnation method and their catalytic performances were tested in the hydrogenation of LA to GVL on a fixed bed reactor. The physicochemical properties of the catalysts were characterized by XRD, H₂-TPR, NH₃-TPD, and BET techniques. The TiO₂ component significantly affected the acidity of the catalyst, and thus its catalytic activity for the GVL yield was affected. The desired product GVL with a yield of about 97% was obtained over the Ru/Al₂O₃–TiO₂ catalyst under mild conditions (WHSV = 1.8 h⁻¹, T = 80 °C). Moreover, the catalyst Ru/Al₂O₃–TiO₂ exhibited excellent thermal stability in the test period of time.

Novel catalytic material with high catalytic activity and hydrothermal stability plays a key role in the efficient conversion of levulinic acid (LA) to γ-valerolactone (GVL) in water.     

Photocatalytic activity of Ag/Al2O3–Gd2O3 photocatalysts prepared by the sol–gel method in the degradation of 4-chlorophenol

The photocatalytic activity in the degradation of 4-chlorophenol (4-ClPh) in aqueous medium (80 ppm) using 2.0 wt% Ag/Al₂O₃–Gd₂O₃ (Ag/Al–Gd-x; where x = 2.0, 5.0, 15.0, 25.0 and 50.0 wt% of Gd₂O₃) photocatalysts prepared by the sol–gel method was studied under UV light irradiation. The photocatalysts were characterized by N₂ physisorption, X-ray diffraction, SEM, HRTEM, UV-Vis, XPS, FTIR and fluorescence spectroscopy. About 67.0% of 4-ClPh was photoconverted after 4 h of UV light irradiation using Ag/γ-–Al₂O₃. When Ag/Al–Gd-x photocatalysts were tested, the 4-ClPh photoconversion was improved and more than 90.0% of 4-ClPh was photoconverted after 3 h of UV light irradiation in the materials containing 15.0 and 25.0 wt% of Gd₂O₃. Ag/Al–Gd-25 was the material with the highest efficacy to mineralize dissolved organic carbon, mineralizing more than 85.0% after 4 h of UV light irradiation. Silver nanoparticles and micro-particles of irregular pentagonal shape intersected by plane nanobelts of Al₂O₃–Gd₂O₃ composite oxide were detected in the Ag/Al–Gd-25 photocatalyst. This material is characterized by a lowest recombination rate of electron–hole pairs. The low recombination rate of photo-induced electron–hole pairs in the Ag/Al–Gd-x photocatalysts with high Gd₂O₃ contents (≥15.0 wt%) confirmes that the presence of silver nanoparticles and microparticles interacting with Al₂O₃–Gd₂O₃ composite oxide entities favors the separation of photo-induced charges (e⁻ and h⁺). These materials could be appropriate to be used as highly efficient photocatalysts to eliminate high concentrations of 4-ClPh in aqueous medium.

Ag/Al₂O₃–Gd₂O₃ showed high efficacy to photodegradate 4-chlorophenol, the strong interaction between silver nano-particles and micro-particles and Al₂O₃–Gd₂O₃ entities favors the decrease in the recombination rate.     

Dehydrocyclization–cracking of methyl oleate by Pt catalysts supported on a ZnZSM-5–Al2O3 hierarchical composite

The dehydrocyclization–cracking of methyl oleate was performed by ZnZSM-5–Al₂O₃ hierarchical composite-supported Pt catalysts in the range of 450–550 °C under 0.5 MPa hydrogen pressure. Most catalysts converted methyl oleate completely and produced aromatics with more than 10 wt% yield as well as valuable fuels even at 450 °C. The reactivity of catalysts changed remarkably depending on the addition method of Pt, while supporting Pt of 0–0.16 wt% did not affect the pore structure of each catalyst. When Pt was introduced into the composite support by the conventional impregnation method, remarkable hydrocracking proceeded through the decarboxylation and decarbonylation of methyl oleate and the successive conversion of C17 fragments and gave the significant amounts of gaseous products. Nevertheless, the selectivity for the aromatics of the gasoline fraction was relatively high and the yields of aromatics reached maximum 19% at 500 °C under 0.5 MPa, suggesting that gaseous olefins would be cyclized through the Diels–Alder reaction on ZnZSM-5 in the composite support. In contrast, when Pt was introduced into catalysts by ion-exchange with ZnZSM-5, the significant conversion of methyl oleate was inhibited and produced liquid fuels in a wide range.

The ideal reaction route in the dehydrocyclization–cracking of methyl oleate catalyzed by Pt/ZnZSM-5–Al₂O₃ is to produce xylene, toluene, and hydrogen through decarboxylation.     

Ni nanocatalysts supported on mesoporous Al2O3–CeO2 for CO2 methanation at low temperature

The selectivity and activity of a nickel catalyst for the hydrogenation of carbon dioxide to form methane at low temperatures could be enhanced by mesoporous Al₂O₃–CeO₂ synthesized through a one-pot sol–gel method. The performances of the as-prepared Ni/Al₂O₃–CeO₂ catalysts exceeded those of their single Al₂O₃ counterpart giving a conversion of 78% carbon dioxide with 100% selectivity for methane during 100 h testing, without any deactivation, at the low temperature of 320 °C. The influence of CeO₂ doping on the structure of the catalysts, the interactions between the mesoporous support and nickel species, and the reduction behaviors of Ni²⁺ ions were investigated in detail. In this work, the addition of CeO₂ to the composites increased the oxygen vacancies and active metallic nickel sites, and also decreased the size of the nickel particles, thus improving the low temperature catalytic activity and selectivity significantly.

The addition of CeO₂ to form Ni composite catalysts increased the oxygen vacancies and active metallic nickel sites thus improving the low temperature CO₂ methanation performance.     

Preparation and spectral characteristics of Tm3+/Ho3+ co-doped TeO2–B2O3–BaO glass

TeO–B₂O₃–BaO glasses with different compositions were prepared by the conventional melt-quenching technique. The spectral properties of Tm³⁺/Ho³⁺ co-doped TeO–B₂O₃–BaO glasses with different doping concentrations were studied. In order to analyze the spectroscopic properties in detail, the Judd–Ofelt intensity parameters, spontaneous radiative probabilities, branching ratios, absorption and emission cross-sections, and gain coefficient spectra were calculated using Judd–Ofelt and McCumber theory based on the absorption and emission spectra. Meanwhile, the optimal doping concentration was determined as Tm₂O₃: 1.0 mol% and Ho₂O₃: 1.0 mol%. The results show that Tm³⁺/Ho³⁺ co-doped TeO–B₂O₃–BaO glass is an ideal mid-infrared laser gain medium.

TeO₂–B₂O₃–BaO glasses with different compositions and Tm³⁺/Ho³⁺ co-doped TeO₂–B₂O₃–BaO glasses with different doping concentrations were prepared and studied.     

Synthesis of a porous SiO2–H3BO3–V2O5–P2O5 glassy composite: structural and surface morphological behaviour for CO2 gas sensing applications

The present work mainly focuses on the fabrication of a porous glass 40SiO₂–35H₃BO₃–19V₂O₅–6P₂O₅via a melt-quenching technique. The structural, morphological, and sensing behaviour of the glass sample was investigated successfully. The calculated density and molar volume of the fabricated glass are 2.4813 ± 0.124 g cm⁻³ and 35.7660 ± 1.708 cm³ mol⁻¹. XRD, SEM and TEM analyses confirmed the amorphous nature of the glass. FTIR results revealed the O–H bond formations, which indicate that the presence of water molecules is probably due to the porous nature of the glass. Further, BET analysis confirmed the mesoporous nature of the glass sample with a mean pore diameter of 7 nm. The sensing response of the synthesized glass at 1000 ppm concentration of CO₂ was found to be 3.05 with a response time 22.6 s and recovery time 25.8 s. Hence, this porous glass can be easily synthesized, is affordable, and was found to be useful for CO₂ gas sensing applications.

The present work mainly focuses on the fabrication of a porous glass 40SiO₂–35H₃BO₃–19V₂O₅–6P₂O₅via a melt-quenching technique.     

Solvothermal synthesis of CeO2–ZrO2–M2O3 (M = La,Y, Bi) mixed oxide and their soot oxidation activity

CeO₂–ZrO₂-M₂O₃ (M = La, Y, Bi) mixed oxide has been prepared by a solvothermal synthesis method. The physico–chemical properties of the mixed oxide have been studied by X-ray powder diffraction (XRD), Raman spectroscopy, BET, X-ray photoelectron spectroscopy (XPS), TEM and temperature-programmed reduction (TPR), and the catalytic activity for soot oxidation has been studied by thermogravimetry (TG). La³⁺, Y³⁺ and Bi³⁺ exhibit positive effects on lowering the oxidation temperature of the soot. The XRD and Raman results showed formation of mixed oxides and TEM images suggested the nanosized nature of the particles. The benefit of yttrium or lanthana doping on the catalytic activity of ceria can be related to active oxygen formation provoked by the defective structure of ceria due to the presence of La³⁺ and Y³⁺. The benefit of Bi³⁺ doping on catalytic activity can be related to the reduction at low temperature both with Bi₂O₃ and ceria.

Nano CeO₂-based oxides with meso-pores have been synthesized by a solvothermal method.