Ascorbic acid-mediated synthesis and characterisation of iron oxide/gold core–shell nanoparticles.

The current article reports on providing surface modification of magnetic nanoparticles with gold to provide stability against aggregation. Gold-coated magnetite nanoparticles were synthesised to combine both magnetic as well as surface plasma resonance (SPR) properties in a single moiety. The nanocomposites were produced by reduction (using ascorbic acid) of gold chloride on to the surface of iron oxide nanoparticles. Ascorbic acid not only acts as a reducing agent, but also the oxidised form of ascorbic acid i.e. Dehydro-ascorbic acid acts as a capping agent to impart stability to as synthesised gold-coated iron oxide nanocomposites. The synthesised nanocomposite was monodispersed with a mean particle size of around 16 nm and polydispersity index of 0.190. X-ray diffraction analysis confirms presence of gold on the surface of magnetite nanoparticles. The synthesised nanocomposites had a total organic content of around 3.2% w/w and also showed a shifted SPR peak at 546 nm as compared to gold nanoparticles (528 nm). Both uncoated and gold-coated magnetite exhibited superparamagnetic behaviour at room temperature. Upon coating with gold shell, saturation magnetisation of iron oxide nanoparticles decreases from 42.806 to 3.54 emu/gram.     

Single-step co-deposition of nanostructured tungsten oxide supported gold nanoparticles using a gold–phosphine cluster complex as the gold precursor

The use of a molecular gold organometallic cluster in chemical vapour deposition is reported, and it is utilized, together with a tungsten oxide precursor, for the single-step co-deposition of (nanostructured) tungsten oxide supported gold nanoparticles (NPs). The deposited gold-NP and tungsten oxide supported gold-NP are highly active catalysts for benzyl alcohol oxidation; both show higher activity than SiO₂ supported gold-NP synthesized via a solution-phase method, and tungsten oxide supported gold-NP show excellent selectivity for conversion to benzaldehyde.     

Synthesis of protein–gold nanoparticle hybrid and gold nanoplates in protein aggregates

A straightforward and economically viable approach was developed to biomimetic synthesis of gold nanocrystals by using casein micelles (CMs) without additional reductant. The UV–vis, TEM, SAED, FTIR, DLS and XRD techniques were employed to systematically characterize Au nanocrystals synthesized. Isotropic gold nanoparticle (GNP) and gold nanoplates in good yields (up to 90%) with different sizes can be obtained easily by adjusting the experimental condition. Spherical nanoparticles were obtained with tunable mean sizes at higher pH and casein concentrations. The high colloidal stability of the spherical GNP is attributed to the formation of CM/GNP hybrid under some experimental condition. At lower pH, reaction temperature and casein concentrations, single-crystalline gold nanoplates in good yields (up to 90%) are obtained. The growth of these nanostructures is attributed to an interplay between the faceting tendency of the protein molecules/micelles and the growth kinetics. More importantly, the morphological evolution of large gold nanoplates at different reaction times has been followed, and compared with some earlier protein systems, different formation mechanisms in casein micelles are obtained. The results demonstrate that both the property of individual protein molecules and protein aggregates play important roles in controlling the formation of gold nanocrystals by using amphiphilic protein.     

Synthesis and characterization of gold–polypyrrole film composite

Polypyrrole (PPy) coatings have potential applications in batteries, fuel cells, sensors, anti-corrosion coatings, and drug delivery systems. In this article, PPy film coating on the electrode of quartz crystal microbalance (QCM) was exposed to acidic aqueous HAuCl₄ solution. The reduction for gold ions took place and gold particles were produced at the film surface. The gold content at the PPy film was monitored by using QCM. The concentration of gold uptake increases as the original concentration of HAuCl₄ solution increases. The morphology of the film before and after the deposition of the gold particles was studied by the scanning electron microscopy coupled with energy dispersive X-ray spectrometry. The gold particles are of undefined shape and have diameters around 200–600 nm. However, the image of the composite powder shows that gold particles of sizes 100–120 nm are distributed over the surface of the polymer particles with some aggregation. Infrared spectroscopy and X-ray diffraction were used to characterize the composite.     

Structure and properties of Titanium–25 Niobium–x iron alloys

The present work studies the effect of iron on microstructure, mechanical properties and corrosion behavior of Ti–25Nb based system with emphasis on improving strength/modulus ratio. Experimental data shows that cast Ti–25Nb–3Fe has a phase with a entirely of dendrite morphology. The bending strength/modulus ratio is 24.6 higher than Ti–6Al–4V (17.4) by 41.4% and than c.p. Ti (9.3) by 165%. The critical anodic current density of the metal in 37 °C Hanks solutions is lower than approximately 100 A/cm². Ti–25Nb–3Fe alloy has a great potential for use as an implant material.     

Influence of molybdenum on austempering behaviour of ductile iron Part 1 – Austempering kinetics and mechanical properties of ductile iron containing 0·13%Mo

Abstract

Measurements of the austempering kinetics and mechanical properties are presented for a ductile iron of composition Fe–3·51C– 2·81Si–0·25Mn–0·39Cu–0·13Mo–0·04Mg (wt-%) for austempering temperatures of 285, 320, 375, and 400°C after austenitising at 870°C for 120 min. The kinetic studies show that the alloying level is insufficient to cause a significant delay in ausferrite formation in the intercellular boundaries. This implies that the heat treatment processing window is open for all austempering conditions studied. The mechanical property measurements show that with the correct selection of austempering temperature all the grades of the ASTM Standard 897M : 1990 and BS EN 1564 : 1997 can be satisfied. The hardenability of the present iron is limited and it is therefore unlikely that these standards will be achieved in thicker section components.     

Microstructure and properties of Ti–Nb–V–Mo-alloyed high chromium cast iron

The correlations of microstructure, hardness and fracture toughness of high chromium cast iron with the addition of alloys (titanium, vanadium, niobium and molybdenum) were investigated. The results indicated that the as-cast microstructure changed from hypereutectic, eutectic to hypoeutectic with the increase of alloy contents. Mo dissolved in austenite and increased the hardness by solid solution strengthening. TiC and NbC mainly existed in austenite and impeded the austenite dendrite development. V existed in multicomponent systems in forms of V alloy compounds (VCrFe₈ and VCr₂C₂). With the increase of alloy additions, carbides size changed gradually from refinement to coarseness, hardness and impact toughness were increased and then decreased. Compared with the fracture toughness (6 J/cm²) and hardness (50·8HRC) without any alloy addition, the toughness and hardness at 0·60 V–0·60Ti–0·60Nb–0·35Mo (wt%) additions were improved and achieved to 11 J/cm² and 58·9HRC, respectively. The synergistic roles of Ti, Nb, V and Mo influenced the solidification behaviour of alloy. The refinement of microstructure and improvement of carbides morphologies, size and distribution improved the impact toughness.     

Effects of Thermal Annealing and Pulsed Photon Processing on the Relaxation and Crystallization of Amorphous Fe–P–Si Alloys

The crystallization behavior of amorphous Fe–P–Si alloys is found to be influenced by preliminary relaxation via thermal annealing below the crystallization temperature T _x or pulsed photon processing with energy densities in the range 1–18 J/cm². High-temperature annealing (above T _x) and pulsed photon processing reduce the particle size and microhardness of the alloys.     

Preparation and conductivity of dithiolene complex Langmuir–Blodgett films

The d.c. electrical property of the dithiolene complex, or bis(4-diethyannodithiobenzil)nickel (BDN) and stearyl alcohol (SA) mixed Langmuir–Blodgett films was investigated. The conductivity of the LB films as a function of the thickness of the films and the ratio of BDN:SA as well as the current versus voltage (I–V) characteristics have been measured. The conductivity of the LB films is about 3.5 x 10^-10 S cm^-1 which is less than the bulk conductivity of BDN, and the conductivity of the LB films is strongly influenced by BDN concentration. The I–V property of Al-LB films is governed by the thickness of oxide layers at the LB films with Al electrodes after Auger depth profiling analysis.     

Microstructural evolution of gold–aluminum wire-bonds

The purpose of this study is to understand the morphological changes that occur during annealing of Al–Au wire-bonds, by analyzing the interface region of annealed model wire-bonded samples between 5N (99.999%) Au wires and Al pads. Due to the small length scale of the intermetallic region at the interface of the bond, the analysis was done using scanning/transmission electron microscopy combined with energy dispersive spectroscopy. Samples were prepared using a dual-beam focused ion beam system. Microstructural characterization showed that during annealing, a Au-rich intermetallic region was formed under the bond and at the periphery of the bond. Two types of failures occurred during annealing: crack formation at the bond periphery due to an increase in volume during intermetallic growth and the formation of stresses; and oxidation of the AlAu₄ phase adjacent to the Au ball, which resulted in the formation of continuous cracks between the Au ball and the intermetallic region. The characteristic void-line found inside the intermetallic region played no part in failure that occurred during exposure to elevated temperatures.     

Investigation of microstructure and mechanical properties of steel fibre–cast iron composites

Abstract

The aim of the present experimental study was to investigate improvement of the toughness and strength of grey cast iron by reinforcing with steel fibres. The carbon content of the steel fibres was chosen to be sufficiently low that graphite flakes behaving as cracks were removed by carbon diffusion from the cast iron to the steel fibres during the solidification and cooling stages. To produce a graphite free matrix, steel fibres with optimum carbon content were used and the reinforced composite structure was cast under controlled casting conditions and fibre orientation. Three point bend test specimens were manufactured from steel fibre reinforced and unreinforced flake graphite cast iron and then normalising heat treatments were applied to the specimens at temperatures of 800 and 850°C. The fracture toughness and strength properties of the steel fibre reinforced material were found to be much better than those of unreinforced cast iron. The microstructures of the composite at the fibre–matrix transition zone were examined.     

Annealing Influence on the Microstructure and Magnetic Properties of Ni–Mn–In Alloys Ribbons

We report on the structure, microstructure and inverse magnetocaloric effect associated with the first-order martensitic phase transition, in Heusler Ni_50.0Mn_35.5In_14.5 alloy ribbons. We have studied the short-time vacuum annealing influence at 1048?K, 1073?K, 1098?K, and 1123?K in these properties. At room temperature, an increase in the degree of structural order for ribbons annealed up to 1098 K was observed, corresponding to cubic L2₁ austenite phase. Meanwhile, for the sample annealed at 1123?K a monoclinic 10M martensitic phase was detected. A comparison of magnetic entropy change as a function of the applied field, after using zero-field-cooling thermomagnetic and isothermal magnetization measurements, has been made for the sample annealed at 1073?K.     

Synthesis of gold nanorods and nanowires by a microwave–polyol method

HAuCl₄ was reduced by ethylene glycol, in the presence of polyvinylpyrrolidone (PVP) under microwave (MW) heating in a continuous wave (CW) mode for 2 min. Dominant products were polygonal nanoplates and close-to-spherical nanoparticles of gold. In addition, small amounts of single crystalline gold nanorods and nanowires (0.5–3% of total number of products) with diameters of 20–100 nm and lengths of 0.6–5 μm were produced. The diameter and length of gold nanorods and nanowires could be controlled by changing the HAuCl₄·4H₂O/PVP ratio. The formation mechanism of anisotropic gold nanostructures was discussed.     

Novel and simple route for the synthesis of core–shell chitosan–gold nanocomposites

This work presents a novel and simple route for the synthesis of water-soluble core–shell chitosan–gold nanocomposites. The experimental procedure can be summarized by the following steps: (i) chitosan deacetylation, (ii) chitosan depolymerization, (iii) chitosan nanoparticles’ formation and (iv) chitosan–gold nanocomposite formation. FT-IR spectroscopic results indicate that the formation of chitosan nanoparticles (ChtNPs) occurs via NH₃⁺ and PO⁻ groups electrostatic interactions, while UV–vis spectra points to a possible embedding of gold nanoparticles into the ChtNPs. This feature was confirmed by electronic transmission microscopy measurements. Chitosan and gold are biocompatible materials. Added to this, the obtained chitosan–gold nanocomposites presented thermal and absorbance properties which strongly point to their potential use in phototherapeutic processes.     

Preparation and complex characterization of silica holmium sol–gel monoliths

Amorphous, sol–gel derived SiO₂ are known to biocompatible and bioresorbable materials. Biodegradable and inert materials containing radioactive isotopes have potential application as delivery vehicles of the beta radiation to the cancer tumors inside the body. Incorporation of holmium in the sol–gel derived SiO₂ could lead to the formation of a biodegradable material which could be used as carrier biomaterial for the radiation of radioactive holmium to the various cancer sites. The homogeneity of the prepared sol–gel silica holmium monoliths was investigated by Back Scattered Electron Imaging of Scanning Electron Microscope equipped with Energy Dispersive X-ray Analysis, X-ray Induced Photoelectron Spectroscopy and Nuclear Magnetic Resonance Spectroscopy. The biodegradation of the monoliths was investigated in Simulated Body Fluid and TRIS (Trizma pre-set Crystals) solution. The results show that by suitable tailoring of the sol–gel processing parameters holmium can be homogeneously incorporated in the silica matrix with a controlled biodegradation rate.     

Plastic accommodation of martensite in disordered and ordered iron–platinum alloys

Abstract

The degree of order in iron–platinum austenite can be changed by heat treatment. Highly ordered austenite tends to transform into thermoelastic martensite, whereas non-thermoelastic martensite isformed from disordered austenite. This is because the ordered austenite is able to accommodate elastically the shape deformation brought about by the growth of martensite. In the present study, atomic force microscopy has been used to establish the nature of the shape deformation caused by both types of martensite. It is confirmed that the extent of plastic accommodation is larger when disordered austenite is induced to transform into martensite.

MST/3232     

Microstructure and mechanical properties of molybdenum–iron–boron–chromium cladding using argon arc welding

The molybdenum–iron–boron–chromium claddings with different Mo/B atomic ratios were produced on Q235 steel using argon arc welding. The microstructure and crystalline phases were studied by optical microscopy, scanning electron microscopy and XRD. In addition, the formation mechanism of hard phase was investigated by thermodynamic calculations and phase diagrams. The results showed that the claddings were composed of the Mo₂FeB₂, M₃B₂ (M: Mo, Fe and Cr) hard phases and σ-FeMoCr solid solution. In addition, calculated results revealed that the M₃B₂, MB and σ-FeMoCr were successively precipitated from the melting pool. Moreover, the maximum microhardness value of the cladding was about 1600 HV_0.5. Wearing test indicated that claddings of lower Mo/B ratios have better wear resistance.     

Biosynthesis of gold nanoparticles using marine bacteria and Box–Behnken design optimization

Gold nanoparticles are exciting materials because of their potential applications in optics, electronics, biomedical, and pharmaceutical fields. In recent years, environmentally friendly, low-cost biosynthesis methods with bio-applicable features have continued to be developed for the synthesis of gold nanoparticles. In the present study, an actinobacterial strain was isolated from the Petrosia ficiformis (Poiret 1798) sponge, which was collected from a marine environment, and the gold nanoparticle synthesis was performed for the first time from the bacteria type belonging to the Citricoccus genus. The synthesis conditions were optimized using the Box–Behnken experimental design, with a statistical method that included three independent variables (temperature, time, and mixture ratio) to affect the synthesis at three levels (+1, 0, and ?1). Accordingly, the conditions proposed for the biosynthesis of gold nanoparticles at the maximum optical density values that are specific for the Citricoccus sp. K1D109 strain were estimated as 35°C temperature, 24?h, and 1/5 mixture ratio (cell-free extract/HAuCl₄?·?3H₂O). When recommended conditions were applied, it was determined that the maximum absorbance of the synthesized gold nanoparticles is 1.258 at 545?nm, and their sizes are in the range of 25–65?nm, according to transmission electron microscopy (TEM) data.     

Effect of multicomponent modifier on microstructure and mechanical properties of high Ni–Cr–Mo cast iron

Abstract

The microstructure and mechanical properties of high Ni–Cr–Mo indefinite chilled cast iron with the addition of a newly developed multicomponent modifier consisting of mixed rare earths, Si–Ca alloy and Bi–Sb alloy have been investigated through optical microscopy, X-ray diffraction and scanning electron microscopy, along with hardness, impact toughness and wear resistance measurements. After the addition of the modifier, the grain sizes of the primary austenite and eutectic carbides are found to be greatly refined, and the typically highly continuous net-like carbides become less interconnected but rather appear more blocky shaped. Such microstructure changes lead to mechanical property improvement in the cast specimen, with its hardness increased from 43 to 50 HRC, impact toughness from 6·3 to 7·8 J cm^?2 and ?20% increase in abrasive wear resistance.