Pyrolysis of ruthenocene carried out in an atmosphere of argon or hydrogen is found to give rise to spherical nanoparticles
of carbon with diameters in the 10–200 nm range. Pyrolysis of ruthenocene as well as mixtures of ruthenocene and ethylene
in hydrogen gives rise to spherical nanoparticles, which contain a high proportion of sp3 carbon. Under certain conditions, pyrolysis of ruthenocene gives rise to graphite coated ruthenium nanoparticles as well
as worm-like carbon structures. Pyrolysis of mixtures of ruthenocene and ferrocene gives rise to nanoparticles or nanorods
of FeRu alloys, the composition depending upon the composition of the original mixture. Nanorods of the Ru and FeRu alloys
encapsulated in the carbon nanotubes are also formed in the pyrolysis reaction. 相似文献
In this study, pure TiO2-nanoparticles and TiO2/sewage sludge (TS) as biomass material were synthesised via a sol–gel method. The adsorption potential of nanosized TiO2 and TS for removal of Cd(II) was investigated in a batch system. The prepared adsorbents were characterised using X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). The XRD analysis showed that pure TiO2 is in amorphous phase before calcination and in anatase phase at annealing temperature of 400 °C. TiO2/sewage sludge that calcined at 400 °C (TS400) was found to be the best adsorbent for cadmium removal from aqueous solution. Kinetic and isotherm studies were carried out by considering the parameters, pH, initial concentration and contact time. The optimum pH value for Cd(II) adsorption onto TS400 was found to be 6. Langmuir isotherm showed better fit than Freundlich isotherm and the maximum adsorption capacity was found to be 29.28 mg/g which is higher than that of many other adsorbents reported in literature. The sorption kinetic data were well fitted with a pseudo-second-order model. These results demonstrated that TS400 was readily prepared and is the promising and effective solid material for the removal of Cd(II) from aqueous solutions. 相似文献
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. 相似文献
A green method for the solvothermal synthesis of copper sulphide nanoparticles (CuS NPs) using xanthan gum as a capping agent was developed. The CuS NPs were characterised by scanning electron microscopy, transmission electron microscopy (TEM), X-ray diffraction, Brunauer–Emment–Teller, zeta analysis, thermal gravimetric– differential thermal analysis, Fourier transform infrared and UV–visible absorption spectra. These characterisations together determine the composition, structural, thermal and optical properties. The UV–visible spectrum had a broad absorption in the visible range. The particle size of the products was observed by TEM in the range of 8–20 nm. The photocatalytic performance of the CuS NPs was evaluated for the degradation of organic dyes (methylene blue, rhodamine B, eosin Y and congo red) under irradiation of solar, visible and UV lights. The CuS NPs showed good photocatalytic activity. Kinetic analyses indicate that the photodegradation rates of dyes usually follow pseudo-first-order kinetics for degradation mechanisms. 相似文献
This work is aimed at developing a green antimicrobial coating. First, a green antimicrobial agent, quaternised chitosan (QCS)/organic montmorillonite (OMMT)/silver nanoparticles (Ag NPs) (QOMA) nanocomposite was fabricated through an environmental-friendly one-step approach. Morphological and structural characteristics of QOMA were investigated, and good antimicrobial activity was proved. QOMA was then incorporated into powder coating formulations to form a homogeneous coating on steel plates, which was studied by scanning electron images. Besides, the physical and mechanical properties as well as the antimicrobial performances of the coatings were discussed. The results showed that the addition of QOMA imparted good antimicrobial capacity to the powder coating, but did not affect its physical and mechanical properties. The coatings were able to effectively inactivate Gram-negative bacteria (Escherichia coli), Gram-positive bacteria (Staphylococcus aureus) and fungi (Aspergillus niger, Penicillium funiculosum, Chaetomium globasum, Paecilomyces varioti, Asp. terreus and Aureobasidium pullulans). Our findings demonstrate the possibilities of green antimicrobial coating containing QOMA for practical applications in medical devices, domestic appliances and other solid surfaces concerning bacterial infection and contamination. 相似文献
In this paper, we describe the facile and effective preparation of a series of cobalt-doped Fe3O4 nanocatalysts via chemical coprecipitation in an aqueous solution. The catalyst allowed the hydrogenation of chloronitrobenzenes to chloroanilines (CAs) to proceed at low temperatures in absolute water and at atmospheric pressure, resulting in approximately 100% yield and selectivity. Several factors that influence the yield of CAs were investigated. The results showed that the suitable dosage of the catalyst was ~10 mol.% of the substrate, and the optimal reaction time, reaction temperature, and reaction pressure were 20 min, 80 °C, and atmospheric pressure, respectively. Under the optimal reaction conditions, the CA yield was as high as 98.4%, and the nitro reduction rate reached 100%, which indicates the excellent selectivity of the homemade catalyst. This process also overcomes the environmental pollution harms associated with the traditional process.
Safe fluorescent gene-transfection vectors are in great demand for basic biological applications and for gene-therapy research. Here, we introduce a new type of luminescent silicon nanoparticle (SiNP)-based gene carrier suitable for determining the intracellular fate of the gene vehicle in a long-term and real-time manner. The presented SiNP-based nanocarriers simultaneously feature strong and stable fluorescence, high DNA-loading capacity and gene-transfection efficiency, as well as favorable biocompatibility. Taking advantage of these unique benefits, we were able to readily observe the behavior of the gene carriers in live cells (e.g. cellular uptake, intracellular trafficking, and endosomal escape) in a long-term and real-time manner. The results demonstrate the potential usability of these fluorescent SiNP-based gene vectors as powerful tools in the field of gene therapy, and provide invaluable information for understanding the intracellular behavior of gene carriers.
Nanoparticles of catalytically important transition metals, such as Pd, Pt, Rh, and Ru have been prepared by the well-known “digestive ripening” (DR) and “modified digestive ripening” (mDR) methods. In the traditional DR process, a polydisperse colloidal dispersion is refluxed in the presence of a surface-active molecule, such as alkanethiol. The mDR method involved a small modification in the procedure, wherein refluxing was performed with an alkanethiol and a tetra-alkylammonium bromide surfactant. This minor modification led to a dramatic change in the final particle size distributions, giving access to nanoparticles in the <3 nm size regime; this was not possible with the traditional DR process. Bromide ions, which are present during refluxing, proved to be an important ingredient in the modification process. These bromide ions are revealed to act as etchants, resulting in ultra-small nanoparticles. All transition metal nanoparticles investigated displayed catalytic activity in the reduction reaction of p-nitro phenol. Pd nanoparticles, synthesized by a modified digestive ripening method, exhibited the best catalytic activity among the systems investigated.
