New organometallic salts as precursors for the functionalization of carbon nanotubes with metallic nanoparticles

New organometallic salts were synthesized in aqueous solution and were used as precursors for the functionalization of carbon nanotubes (CNT) by metallic nanoparticles. The precursors were obtained by reaction between HAuCl₄, (NH₄)₂PtCl₆, (NH₄)₂PdCl₆, or (NH₄)₃RhCl₆ with cetyltrimethylammonium bromide (CTAB). The as-obtained (CTA) _n Me _x Cl _y salts (with Me?=?Au, Pt, Pd, Rh) were characterized by Fourier-transform infra-red (FTIR) spectroscopy, ¹H nuclear magnetic resonance (NMR) spectroscopy, and thermogravimetric analysis. These precursors were then used to synthesize metallic nanoparticles of Au, Pt, Pd, and Rh over multiwalled carbon nanotubes (MWCNT). Characterization by scanning transmission electron microscopy (STEM) and thermogravimetric analysis under air reveals that the CNT-supported catalysts exhibit high loading and good dispersion of the metallic nanoparticles with small average particle sizes. The present preparation procedure therefore allows obtaining high densities of small metallic nanoparticles at the surface of MWCNT.     

Preparation of stimuli-responsive nanogels based on poly(N,N-diethylaminoethyl methacrylate) by a simple “surfactant-free” methodology

The synthesis of poly(N,N-diethylaminoethyl methacrylate)-core-polyethyleneglycol-shell (PDEAEM-core-PEG-shell) nanogels was achieved by using a “surfactant-free” emulsion polymerization with the aid of commercially available polyethyleneglycol methyl ether methacrylates (PEGMAs) as polymerizable stabilizers. By adjusting the synthetic parameters like the choice of initiator, cross-linker, PEGMA:DEAEM ratio, and molecular weight of PEGMA, a series of core-shell nanogels varying in size (50–350 nm), PDEAEM content, and pH/temperature responsive behavior were obtained in reactions taking only 60 min. The nanogels were used as nanoreactors for the preparation of gold nanoparticles. The PEGylated nanogels have a great potential to be used for diagnosis and therapy.     

Effect of γ-irradiation on the growth of ZnO nanorod films for photocatalytic disinfection of contaminated water

The growth of ZnO nanorods on a flat substrate containing γ-irradiated seeds and their ability to photocatalytically eliminate bacteria in water were studied. The seed layer was obtained, by the spray pyrolysis technique, from zinc acetate solutions γ-irradiated within the range from 0 to 100 kGy. Subsequently, to grow the rods, the seeds were immersed in a basic solution of zinc nitrate maintained at 90 °C. The rate of crystal growth on the seed layer during the thermal bath treatment was kept constant. The resulting materials were characterized morphologically by scanning electron and atomic force microscopies; X-ray diffraction was used to study their morphology and structure and ultraviolet-visible spectroscopy to determine their absorbance. The obtained seed films were morphologically dependent on the radiation dose and this was correlated with the ZnO nanorod films which presented a texture in the (002) direction perpendicular to the substrate. The rods have a hexagonal mean cross section between 20 and 140 nm. Using these rods, the photocatalytic degradation of Escherichia coli bacteria in water was studied; a positive influence of the crystalline texture on the degradation rate was observed.     

Influence of organic solvents in the Pt nanoparticle synthesis on MWCNT for the methanol oxidation reaction

Journal of Solid State Electrochemistry - We studied the effect of the organic solvent on the synthesis of platinum nanoparticles anchored on the surface of multi-wall carbon nanotubes (Pt...     

Ratiometric arginine assay based on FRET between CdTe quantum dots and Cresyl violet

The authors report on the design of a new Förster resonance energy transfer (FRET) based ratiometric nanoprobe for the determination of arginine. The method is based on the inhibition of the efficiency of FRET in assemblies formed between CdTe quantum dots capped with mercaptopropionic acid (QD-MPA) acting as energy donor, and the dye Cresyl Violet (CV) that acts as an energy acceptor at pH 8. Addition of arginine causes a displacement of the CV by arginine on the surface of the QD/MPA. Hence, the FRET between QD/MPA and CV is interrupted and fluorescence emission of the donor (QD/MPA) is restored. Arginine selectively binds to the QD/MPA via electrostatic and hydrogen bonding interactions between guanidinium and carboxylate. Under optimum conditions, the ratio of the fluorescence emissions peaking at 575 and 620 nm (under 400 nm excitation) is linear in the 1 to 30 μM arginine concentration range, and the detection limit is 0.51 μM. The nanoprobe displays good selectivity over 14 other amino acids, many metal ions, glucose, and ascorbic, tartaric and citric acids. The fluorescent nanoprobe was successfully applied to the determination of arginine in pure and spiked real samples and gave good recoveries. Its good selectivity, sensitivity, low-cost and rapidity make the QD-dye assembly a suitable nanoprobe for the quantitation of arginine.

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Graphical abstract Schematic of a FRET ratiometric nanoprobe for arginine. It is based on quantum dots acting as energy donors and Cresyl Violet acting as energy acceptor. The FRET process is interrupted by the addition of arginine which selectively interacts with carboxy groups via a guanidinium-carboxylate salt bridge.

     

h-MoO3 phase transformation by four thermal analysis techniques

Journal of Thermal Analysis and Calorimetry - Molybdenum trioxide (MoO3) has been studied by four thermal analysis techniques. The as-synthesized material has hexagonal structure (h-MoO3). The...