A simple route to incorporate redox mediator into carbon nanotubes/Nafion composite film and its application to determine NADH at low potential

Through a new and simple ion-exchange route, two-electron redox mediator thionine has been deliberately incorporated into the carbon nanotubes (CNTs)/Nafion composite film due to the fact that there is strong interaction between any of two among the three materials (ion-exchange process between thionine and Nafion, strong adsorption of thionine by CNTs, and wrapping and solubilizing of CNTs with Nation). The good homogenization of electron conductor CNTs in the integrated films provides the possibility of three-dimensional electron conductive network. The resulting integrated films exhibited high and stable electrocatalytic activity toward NADH oxidation with the significant decrease of high overpotential, which responds more sensitively more than those modified by thioine or CNTs alone. Such high electrocatalytic activity facilitated the low potential determination of NADH (as low as -0.1 V), which eliminated the interferences from other easily oxidizable species. In a word, the immobilization approach is very simple, timesaving and effective, which could be extended to the immobilization of other cationic redox mediators into the CNTs/Nafion composite film. And these features may offer potential promise for the design of amperometric biosensors.

Extending electrochemical activity of polyaniline to alkaline media via electrostatic interaction and sol-gel route

The electroactivity of polyaniline was extended to pH = 14 alkaline media by preparation of a novel electrostatic interaction conductive hybrid from water-borne conductive polyaniline and silica network containing carboxyl groups via sol-gel process. In addition, the obtained conductive polyaniline hybrid film displayed very low conductivity threshold percolation and demonstrated excellent stability upon cycling.

A simple and effective route for the preparation of poly(vinylalcohol) (PVA) nanofibers containing gold nanoparticles by electrospinning method

Poly(vinyl alcohol) (PVA) nanofibers containing gold nanoparticles have been simply obtained by electrospinning a solution containing gold nanoparticles without the additional step of introducing other stabilizing agents. The optical property of gold nanoparticles in PVA aqueous solution was observed by UV-visible absorption spectra. Morphology of the Au/PVA nanofibers and distribution of the gold nanoparticles were characterized by transmission electron. microscopy (TEM). The structure transformation was characterized from PVA to PVA/Au composite by Fourier transform infrared spectroscopy (FTIR).

In situ synthesis of silica gel nanowire/Na+-montmorillonite nanocomposites by the sol-gel route

Silica-gel nanowire/Na+-montmorillonite (Na+-MMT) nanocomposites were prepared by the in situ sol-gel process of tetraethyl orthosilicate (TEOS) in the presence of Na+-MMT and ammonia as catalyst. Microstructure characterization of the nanocomposites was done by SEM, , EDX, XRD and FTIR. It was found that a lot of silica-gel nanowires grew along the edges of Na+-MMT. The combination between the nanowires and Na+-MMT was accomplished via polycondensation of the hydrolyzed TEOS and the edge-OH groups of Na+-MMT.

Large scale, templateless, surfactantless route to rapid synthesis of uniform poly(o-phenylenediamine) nanobelts

We reported the interesting finding that large scale uniform poly(o-phenylenediamine) nanobelts with several hundred micrometers in length, several hundred nanometers in width, and several ten nanometers in height can be rapidly yielded from an o-phenylenediamine-HAuCl4 aqueous solution without the additional introduction of other templates or surfactants at room temperature.

A novel route to polyethylene-polystyrene blends through the fragmentation of porous polystyrene beads supported metallocene in ethylene polymerization

Polyethylene-polystyrene blends were synthesized by in situ ethylene polymerization with polystyrene porous beads supported metallocene; the influence of fragmenting support beads on the morphology and the mechanical performance of the blends was investigated.

A new route to control product selectivity in the oxidative dehydrogenation of cyclohexane and cyclohexene

The product selectivity can be controlled by adding acetic acid in feed over vanadium phosphate (VPO) in gas phase oxidative dehydrogenation (ODH), in which cyclohexane and cyclohexene are oxidized to cyclohexene and 1,3-cyclohexadiene (1,3-CHD), respectively, at almost 100% selectivity. This approach is also an efficient method to capture the very unstable intermediates in the mechanism study.

Rapid self-assembly of oligo(o-phenylenediamine) into one-dimensional structures through a facile reprecipitation route

The self-assembly of oligo(o-phenylenediamine) (OPD) into 1-D nanostructures on a macroscopic length scale was found when they were transferred from N-methyl pyrrolidone to deionized water. Field emission scanning electron microscopy and confocal fluorescence microscopy were used to investigate the morphology of the precipitates. Results showed that large amounts of OPD 1-D supertructures could be obtained through the simple reprecipitation route, and the length of the fibers could be tuned from microscale to macroscale by adjusting the ratio of two solvents. X-ray diffraction patterns and UV-vis spectra revealed that pi-pi interactions between OPD molecules that facilitated the formation of 1-D structures became predominant when they were transferred from a good solvent to a bad one. Accordingly, a possible formation mechanism was proposed.

Double propagation based on diepoxide, a facile route to high molecular weight poly(propylene carbonate)

Poly(propylene carbonate) (PPC) with number average molecular weight (M-n) higher than 200 kg/mol was prepared via the terpolymerization of carbon dioxide, propylene oxide and diepoxide using Y(CCl3OO)(3)-ZnEt2-glycerine coordination catalyst. When equimolar ZnEt2 and diepoxide were used, double propagation active species were generated in situ by nucleophilic attack of metal alkoxide on diepoxide, leading to PPC of doubled M-n value. The molecular weight of PPC has dramatic influence on its thermal and mechanical performances. PPC with M of 227 kg/mol showed modulus of 6900 MPa, while the modulus of PPC with M-n of 109 kg/mol was only 4300 MPa. Moreover, when M-n increased from 109 to 227 kg/mol, a 37 degrees C increase of the onset degradation temperature was observed.

Synthesis and characterization of ultrafine CeF3 nanoparticles modified by catanionic surfactant via a reverse micelles route

In this article, we firstly reported on the synthesis and characterization of ultratine CeF3 nanoparticles (NPs) modified by catanionic surfactant via a reverse micelles-based route. The catanionic surfactant PN was prepared by mixing the di(2-ethylhexyl) phosphoric acid (DEHPA) and primary amine (N1923) with 1:1 molar ratio. It exhibited a high surface activity and formed much small reverse micelles in comparison with its individual component (DEHPA or N1923). The PN reverse micelles were then used as templates to prepare ultrafine CeF3 NPs. The narrow distributed nanoparticles have an average diameter 1.8 nm. FTIR spectra indicated that there existed strong chemical interactions between nanoparticles and the adsorbed surfactants. The modification resulted in the FFIR peak position of P=O shifting to lower energy. Due to the effect of modification and small size, the CeF3 NPs showed a remarkable red shift of 54 mn in the fluorescence emission in comparison with that of bulk material and a red shift of 18 nm in contrast with that of the normal CeF3 NPs with an average diameter of 16 nm.