Biosynthesis of tin oxide (SnO2) nanoparticles using jujube fruit for photocatalytic degradation of organic dyes

In this study, tin oxide (SnO₂) nanoparticles were synthesized via a green route using jujube fruit as a non-toxic, renewable reducing agent, and excellent stabilizer. The biosynthesized SnO₂ nanoparticles were characterized by X-ray diffraction analysis (XRD), Fourier-Transform infrared (FT-IR), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). Moreover, the photocatalytic activity of the novel SnO₂ nanoparticles was investigated for degradation of two organic dyes which were named methylene blue (MB) and eriochrome black-T (EBT) under direct sunlight. An excellent performance was observed and about 90% and 83% of degradation efficiencies were achieved for MB and EBT, respectively. The high stability of the photocatalyst also makes SnO₂ nanoparticles easily to reuse at least four times without any remarkable loss in activity.     

Hydrothermal synthesis of surface-modified iron oxide nanoparticles

We synthesized surface-modified iron oxide nanoparticles in aqueous phase by heating an aqueous solution of iron sulfate (FeSO₄) at 473 K with a small amount of either n-decanoic acid (C₉H₁₉COOH) or n-decylamine (C₁₀H₂₁NH₂), which is not miscible with water at room temperature. Transmission electron microscopy showed that the addition of n-decanoic acid or decylamine changed the shape of the obtained nanoparticles. X-ray diffraction spectra revealed that the synthesized nanoparticles were in α-Fe₂O₃ or Fe₃O₄ phase while Fourier transform infrared spectroscopy and thermogravimetry indicated the existence of an organic layer on the surface of the nanoparticles. In the synthetic condition, decreased dielectric constant of water at higher temperature increased the solubility of n-decanoic acid or n-decylamine in water to promote the reaction between the surface of iron oxide nanoparticles and the organic reagents. After the synthesis, the used organic modifiers separated from the aqueous phase at room temperature, which may help the environmentally benign synthesis of surface-modified metal oxide nanoparticles.     

Highly enhanced and stable activity of defect-induced titania nanoparticles for solar light-driven CO2 reduction into CH4

Photocatalytic reduction of CO₂ to fuel offers an exciting opportunity for helping to solve current energy and global warming problems. Although a number of solar active catalysts have been reported, most of them suffer from low product yield, instability, and low quantum efficiency. Therefore, the design and fabrication of highly active photocatalysts remains an unmet challenge. In the current work we utilize hydrogen-doped, blue-colored reduced titania for photocatalytic conversion of CO₂ into methane (CH₄). The photocatalyst is obtained by exposure of TiO₂ to NaBH₄ at 350 °C for 0.5 h. Sensitized with Pt nanoparticles, the material promotes solar spectrum photoconversion of CO₂ to CH₄ with an apparent quantum yield of 12.40% and a time normalized CH₄ generation rate of 80.35 μmol g^?1 h^?1, which to the best of our knowledge is a record for photocatalytic-based CO₂ reduction. The material appears intrinsically stable, with no loss in sample performance over five 6 h cycles, with the sample heated in vacuum after each cycle.     

Interfacial assembly of partially hydrophobic silica nanoparticles induced by ultrasonic treatment

A sonochemical approach has effectively been applied to prepare aqueous dispersions of air-filled nanostructured quartz silica shells from surface-engineered amorphous silica nanoparticles. The non-equilibrium nature of the cavitation process and high temperature and pressure in the cavitation microbubble can lead to partial crystallization of the amorphous silica nanoparticles producing the quartz phase and a high degree of interconnection between the silica nanoparticles in the microsphere shells. The very high stability of the silica shells against collapse and aggregation is determined by the hydrophobic nature of the silica nanoparticles. Because of the shell thickness and its high density caused by sintering of the silica nanoparticles, the gas (liquid) permeability through the shell is limited thus prolonging the life time of the air-filled nanostructured silica shells.     

Facile synthesis of porous hollow iron oxide nanoparticles supported on carbon nanotubes

Porous hollow iron oxide nanoparticles (PHNPs) supported on carbon nanotubes (CNTs) were facilely synthesized by etching Fe@Fe_xO_y/CNT with dilute nitric acid aqueous solution at ambient temperature without the assistance of any surfactants and ligands. The mean diameter of hollow iron oxide nanoparticles was about 17 nm, with a wall thickness of about 4 nm. The formation mechanism of PHNPs is discussed based on the characterization results from TEM, XRD and H₂-TPR. The combination of nanoscale Kirkendall effect and selective acid etching is proposed to be responsible for the formation of CNT supported PHNPs, through a transformation from core/void/shell structures to hollow nanoparticles.     

Multifunctional iron and iron oxide nanoparticles in silica

Iron and iron oxide nanoparticles in silica layers deposited by sol–gel techniques on Si wafers were formed and studied. It was shown that multifunctional nanoparticles of different iron oxides possessing various physical properties can be fabricated by means of post-growth annealing of (SiO₂:Fe)/SiO₂/Si samples in various atmospheres. The hematite, maghemite, and iron nanoparticles were found to be dominant upon annealing the samples in air, argon, and hydrogen atmosphere, respectively. The physical properties of produced hybrid structures were studied by Raman and FT-IR spectroscopy, spectroscopic ellipsometry, AFM, and magnetic measurements. The sol–gel technique with subsequent annealing procedure is demonstrated to be an effective method for the formation of multifunctional hybrid structures composed of iron or iron oxide nanoparticles in silica matrix.     

Effect of heat treatment on ultrasonic velocity in ductile cast iron

Abstract

The measurement of the ultrasonic velocity is a common method in the foundry industry for the evaluation of the nodularity in ductile iron castings. Practical experience has shown that heat treatment can reduce the ultrasonic velocity compared to the as cast condition. Using ductile iron samples with different heat treatments in order to vary the ferrite and pearlite content respectively confirmed this decrease in the ultrasonic velocity compared to the as cast state. Further investigations showed that with all the heat treatments applied, irrespective of their effect on the microstructure, the density was decreased. The decrease in density correlated with the decrease in ultrasonic velocity for all heat treatments. The mechanisms involved in the reduction in the density are discussed.     

Superparamagnetic iron oxide nanoparticles assembled magnetic nanobubbles and their application for neural stem cells labeling

Micro/nanobubbles for use as ultrasound contrast agents have been fabricated with different shell materials.When various biomedical nanoparticles have been embedded in the shells of bubbles,the composite structures have shown promising applications in multi-modal imaging,drug/gene delivery,and biomedical sensing.In this study,we developed a new gas-liquid interface self-assembly method to prepare magnetic nanobubbles embedded with superparamagnetic iron oxide nanoparticles(SPIONs).The diameter of the generated assembled nanobubbles was 227.40±87.21 nm with a good polydispersity index(PDI)of 0.29.Under the condition of 150 compression cycles,the nanobubble concentration could reach about 6.12×10⁹/mL.Transmission electron microscopy(TEM)and scanning electronic microscopy(SEM)demonstrated that the assembled nanobubbles had a hollow gas core with SPIONs adsorbed on the surface.Ultrasound(US)imaging and magnetic resonance imaging(MRI)experiments indicated that the assembled magnetic nanobubbles exhibited good US and MR contrast capabilities.Moreover,the assembled magnetic nanobubbles were used to label neural stem cells under ultrasound exposure.After 40 s US exposure,the magnetic nanobubbles could be delivered into cells with 2.80 pg Fe per cell,which could be observed in the intracellular endosome by TEM.Compared with common incubation methods,the ultrasound exposure method did not introduce the potential cytotoxicity of transfection reagents and the efficiency was about twice as high as the efficiency of incubation.Therefore,the assembled magnetic nanobubbles prepared through the pressure-driven gas-liquid interface assembly approach could be a potential US/MRI dual model imaging nanocarrier for regenerative applications.     

Preparation and characterization of Cu3Sn nanoparticles via a facile ultrasonic irradiation

Cu₃Sn nanoparticles were prepared with ease by allowing bulk tin to react with copper acetate under ultrasonic irradiation. The microstructure and thermal stability of resultant Cu₃Sn nanoparticles were analyzed by means of transmission electron microscopy (TEM), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). In the meantime, the possible growing mechanism of Cu₃Sn nanoparticles was presented; and the tribological properties of Cu₃Sn nanoparticles as lubricating additives were evaluated. It has been found that as-synthesized hexagonal Cu₃Sn nanoparticles are of spherical shape and have a narrow size distribution and an average diameter of 90 nm. The growth of Cu₃Sn nanoparticles involves three stages of ultrasonic dispersion, reaction and surface modification. Besides, ultrasonic irradiation in combination with surface-capping by oleic acid contributes to prevent on-growing Cu₃Sn nanoparticles from aggregation, making it feasible for Cu₃Sn nanoparticles to be well dispersed in lubricating base stock and significantly increase the antiwear ability and load-carrying capacity of liquid paraffin.     

Microwave-assisted synthesis and characterization of tin oxide nanoparticles

Tin oxide nanoplatelets (SnO) and nanoparticles (SnO₂) were prepared by microwave assisted technique with an operating frequency of 2.45 GHz. This technique permits to produce gram quantity of homogeneous nanoparticles in just 10 min. The crystalline size was evaluated from XRD and found to range from 26 to 34 nm. SEM and TEM analyses showed that the nanoparticles present a platelet-like shaped particle or, a pseudo spherical morphology, after calcination at moderate temperature during which the phase transformation from SnO to SnO₂ takes place. Additional FT-IR, density and resistivity measurements were also presented.     

Silica coated hard-magnetic strontium hexaferrite nanoparticles

Stable colloids of hard magnetic particles are newly developed and very promising materials. Surface functionalization of these particles remains challenging because the particles tend to aggregate during reaction due to strong magnetic interactions. Herein we report on a synthesis of strontium hexaferrite hard magnetic nanoparticles coated with silica by hydrolysis of tetraethoxysilane. As a source of hexaferrite we used stable colloid of plate-like nanoparticles with mean diameter of 40 nm and thickness of 5 nm, which were prepared by a glass-ceramic process. We have shown that to successfully coat each hexaferrite particle individually the hydrolysis conditions should provide heterogeneous nucleation of silica with rate higher than the aggregation rate of the colloidal nanoparticles. The resulting materials represent single crystal hexaferrite cores wrapped in silica shell with mean thickness of 18 and 23 nm depending on synthesis conditions. The obtained core-shell particles can be easily dispersed as stable aqueous colloids. The materials can be used as magnetic sorbents or nanocontainers and, furthermore, they are very promising colloidal building blocks for various magnetically assembled nanostructures.     

Effect of chloride ion on crystalline phase transition of iron oxide produced by ultrasonic spray pyrolysis

Ultrafine spherical Fe₂O₃ powders with controllable morphology and crystal phase were synthesized by ultrasonic spray pyrolysis. In this experiment, we chose three common ferric salts (Fe(NO₃)₃·9H₂O, FeSO₄·7H₂O or FeCl₂·4H₂O) as precursor solution and regulated the concentration of chlorine ion (Cl^?) in precursor solution to produce Fe₂O₃ particles. The morphology, crystal structure and magnetic property of prepared Fe₂O₃ particles were examined by scanning electron microscopy (SEM), X-ray diffraction (XRD) and Vibrating sample magnetometer (VSM). The diameter of the obtained Fe₂O₃ products ranged from 0.2 to 2?μm. And the product obtained from FeCl₂ precursor solution was magnetic, which was composed of hexagonal α-Fe₂O₃ and cubic γ-Fe₂O₃ from XRD results. We also calculated the weight percent of α-Fe₂O₃ and γ-Fe₂O₃ in the product through XRD quantitative analysis. However, with the addition of Cl^? in Fe(NO₃)₃ or FeSO₄ precursor solution, the products turned from non-magnetic to magnetic, whose pure α-Fe₂O₃ phase became to α-Fe₂O₃ and γ-Fe₂O₃ multi-phase. Besides, the weight percent of γ-Fe₂O₃ and the amount of M_s increased with the Cl^? concentration in precursor solution improving. According to the research, it can be inferred that the presence of Cl^? inhibits the phase transition of γ-Fe₂O₃ to α-Fe₂O₃ at high temperature.     

Melting of iron nanoparticles embedded in silica prepared by mechanical milling

For decades, experimental studies on the size-dependent melting of metals are regretfully limited to some eight archetypal examples. In this work, to expand this slim range of materials, the melting behavior of Fe nanoparticles embedded in SiO₂ prepared by using mechanical milling are investigated. Effects of factors in sample preparation on the size, isolation and thermal stability of Fe nanoparticles are systematically studied. On this basis, the size-dependent melting of Fe is successfully traced: for Fe nanoparticles with a diameter of about 15 nm, the melting point depression is 30 °C in comparison with bulk Fe, in accordance with our recent theoretical prediction.     

Gas-chromism in ultrasonic spray pyrolyzed tungsten oxide thin films

A simple and inexpensive ultrasonic spray pyrolysis (USP) technique has been employed to deposit tungsten oxide (WO₃) thin films by spraying 2.0 mM aqueous ammonium metatungstate solution onto the amorphous glass substrates kept at 250°C. The films were further annealed at 400°C for 4 h in air. X-ray diffraction (XRD) technique was used to determine the crystallinity and to identify the WO₃ phases. It was found that the films were sub-stoichiometric, WO_3-z. To study gas-induced properties, a catalyzing layer of platinum (Pt) was sputtered onto it. The gas-induced electrical and optical properties of Pt/WO₃/glass samples were studied and results reported. It was found that electrical resistivity decreased by a factor of 10 within 2 min and stabilized after 15 min, after H₂ gas exposure. Similarly the optical transmittance of the samples attenuated from 55% to 10% within 15–20 min. The reversible changes in electrical resistivity and optical transmittance were observed when the samples were exposed to oxygen. The response times and sensitivity of the samples were estimated.     

Atomic layer deposition of iron(III) oxide on zirconia nanoparticles in a fluidized bed reactor using ferrocene and oxygen

Conformal films of amorphous iron(III) oxide and α-Fe₂O₃ have been coated on zirconia nanoparticles (26 nm) in a fluidized bed reactor by atomic layer deposition. Ferrocene and oxygen were alternately dosed into the reactor at temperatures between 367 °C and 534 °C. Self-limiting chemistry was observed via in situ mass spectrometry, and by means of induced coupled plasma-atomic emission spectroscopy analysis. Film conformality and uniformity were verified by high resolution transmission electron microscopy, and the growth rate was determined to be 0.15 Å per cycle. Energy dispersive spectroscopy, X-ray diffractometry, and X-ray photoelectron spectroscopy were utilized as a means to determine film composition at each deposition temperature. Over all of the deposition temperatures investigated, films were deposited as amorphous iron(III) oxide. However, after heat treatment at 850 °C in air and N₂ atmospheres, α-Fe₂O₃ was the predominant species.     

Multifunctional use of magnetite-coated tuff grains in water treatment: Removal of arsenates and phosphates

Natural filtration material tuff (T) was modified by coating with nano-sized magnetite. The grain fraction of 0.6–1.9 mm was submitted to hydrothermal synthesis of magnetite. Thus formed magnetite modified tuff (MMT) was characterized in terms of Fe-content, N2 adsorption- desorption isotherm, SEM, zeta potential-pH analyses and adsorption behavior towards phosphates/arsenates in batch and column conditions. Elemental analysis showed that 36.54 mg g^?1 of magnetite was attached to the porous tuff grains. This modification changed pore structure and specific surface area. An increase of cca 35% in Sp value was obtained. Batch experiments proved that MMT was 4-5 times more efficient in removal of phosphates/arsenates than non-modified T. The maximum sorption capacities of phosphates calculated based on Langmuir equation were 0.45 and 1.91 mg g^?1, while those for arsenate were 0.551 m g^?1 and 2.36 mg g^?1 for T and MMT, respectively.The intra-particle diffusion model was the most suited for describing the adsorption process of phosphate and arsenate onto MMT.Fixed-bed column data corroborated batch results, i.e. MMT was 6 times superior in contaminant adsorption than T. Modification with magnetite improved T potential for usage in water treatment applications: its filtration ability remained unchanged, while adsorption capacity for phosphates/arsenates removal was improved.     

Hazard reduction for the application of titania nanoparticles in environmental technology

Photocatalytically active titania (TiO2) nanoparticles are applied, and considered for application, in the degradation of hazardous substances. However, these nanoparticles are also hazardous by themselves. High efficiency immobilization of TiO2 nanoparticles on large inorganic supports that are not vulnerable to photocatalytic degradation is conducive to hazard reduction. Immobilization should also aim at minimizing the release of TiO2 nanoparticles from such supports due to attrition. In doing so there may be a trade off between hazard and photocatalytic activity.     

Erosion characteristics and failure mechanism of reservoir rocks under the synergistic effect of ultrasonic cavitation and micro-abrasives

Ultrasonic cavitation erosion of reservoir rocks in distilled water with and without SiO₂ micro-abrasives (mean diameter 0.5 μm, mass concentration 1–7 wt%) are conducted. The erosion characteristics of eroded rocks are measured and analyzed. Both the area of cavitation damage zones and the surface roughness are increased when rocks are eroded in water-abrasive mixture. Compared with distilled water, the mass loss in 3 wt% water-abrasive mixture has improved by 69.66–104.23% (average 81.41%) for sandstone, 495.05–665.15% (average 557.38%) for shale, and 158.49–211.92% (average 188.16%) for granite during an erosion time of 5 ∼ 60 min. The promoted erosion can be explained by the synergistic effect of cavitation and micro-abrasives. The failure mechanisms are elucidated for different types of rocks. The erosion of reservoir rocks results from the peeling-off of mineral grains and the breakdown of large mineral crystals. Numerous micro-fractures and pores are produced in the surface of the eroded rocks, creating additional permeable channels for fluid flow. The results demonstrate that the presence of micro-abrasives can increase the ultrasonic cavitation erosion of reservoir rocks, indicating that the addition of micro-abrasives is feasible to enhance the performance of ultrasonic treatment for oil wells in petroleum industry.     

Synthesis and characterization of iron oxide nanoparticles dispersed in mesoporous aluminum oxide or silicon oxide

Iron oxide nanoparticles dispersed in aluminum (Al) or silicon (Si) oxides were prepared via a polymeric precursor derived from the Pechini method. The samples were characterized by thermogravimetric analysis, Fourier-transform infrared spectroscopy, X-ray diffraction, N₂ adsorption/desorption isotherms (Brunauer–Emmett–Teller, BET), M?ssbauer spectroscopy, and vibrating sample magnetometry (VSM). BET analysis shows that the samples are mesoporous materials and have a high surface area. The size of the Fe₂O₃ nanoparticles in Al₂O₃ is smaller than that in SiO₂. M?ssbauer spectra of the samples show that the Fe₂O₃ nanoparticles in Al₂O₃ are non-magnetic at room temperature but magnetic below 50 K. The FeSi samples are magnetic at both room and low temperatures. The magnetic measurements with VSM confirmed this point.     

Microstructural evolution of iron oxide hollow nanoparticles toward iron oxide nanotubes in a prolonged sintering condition

Prolonged sintering of iron oxide hollow nanoparticles (HNPs) during chemical vapor condensation (CVC) at 800 °C for 6 h showed some interesting morphologies of the iron oxide nanotubes. TEM and XRD studies confirmed that single-walled nanotubes of a mixed phase of α, β, and γ-Fe₂O₃, with a wall thickness of less than 10 nm and an outer diameter of approximately 50 nm were synthesized. The formation of iron oxide nanotubes was thought to be an evolution of iron oxide HNPs based on the sintering.