Four different samples of ferrocene-grafted hydroxyl-terminated polybutadiene (Fc-HTPB), containing 0.20, 0.52, 0.90, and 1.50 wt % iron, were synthesized by the Friedel-Crafts alkylation of ferrocene with hydroxyl-terminated polybutadiene (HTPB) in the presence of AlCl 3 as a (Lewis acid) catalyst. The effects of the reaction conditions on the extent of ferrocene substitution were investigated. The Fc-HTPBs were characterized by IR, ultraviolet-visible, 1 H-NMR, and 13 C-NMR spectra. The iron content and number of hydroxyl groups were estimated, and the properties, including thermal degradation, viscosity, and propellant burning rates (BRs), were also studied. The thermogravimetric data indicated two major weight loss stages around 395 and 500 C. These two weight losses were due to the depolymerization and decomposition of the cyclized product, respectively, with increasing temperature. The Fc-HTPB was cured with toluene diisocyanate and isophorone diisocyanate separately with butanediol-trimethylolpropane crosslinker to study their mechanical properties. Better mechanical properties were obtained for the gumstock of Fc-HTPB polyurethanes with higher NCO/OH ratios. The BRs of the ammonium perchlorate (AP)-based propellant compositions having these Fc-HTPBs (without dilution) as a binder were much higher (8.66 mm/s) than those achieved with the HTPB/ AP propellant (5.4 mm/s).

No abstract

A new family of chitosan-cross-linked osmium polymer composites was prepared and its electrochemical properties were examined. The composites were prepared by quaternization of the poly(4-vinylpyridine) osmium bipyridyl polymer (PVP-Os) which was then cross-linked with chitosan, yielding PVP-Os/chitosan. Films made of the composites showed improved mass and electron transport owing to the porous and hydrophilic structure which is derived from the cross-links between the Os polymer and chitosan. The rate for glucose oxidation was enhanced four times when glucose oxidase (GOx) was immobilized on PVP-Os/chitosan compared immobilization on PVP-Os.

Ferrocene was linked to polyvinyl alcohol polymer via ethylene dioxi‐bis‐ethylamine (PV‐Fc) spacer and the synthesized redox polymer was characterised by FT‐IR and H1NMR spectroscopy. Aqueous solution of PVA‐Fc was used to prepare its silica composite with tetraethylorthosilicate (TEOS). The immobilized PVA‐Fc/silica film showed E0 about 0.245 V and apparent diffusion coefficient was measured to be 2.76×10−8 cm2 s−1. The ferrocene with flexible spacer in PVA‐Fc/silica film showed an excellent electrocatalytic activity towards the sulfite oxidation at 0.35 V, that was minimum 0.3 V negative shift of the overpotential than the bare electrode. The effect of the interfearing species like acetate, ammonium, carbonate, phosphate and sulfate has been checked for the sulfite detection. Under the optimized conditions the prepared composite showed sulfite oxidation in the linear range of 5×10−7 M to 1×10−4 M and lower detection limits of 1.5×10−7 M.

The development of non-precious metal based electrocatalysts is highly desired for the oxygen reduction reaction (ORR) as alternates to noble metal based ORR electrocatalysts. Herein, we report mononulcear copper(II) complex [CuLbpy]ClO 4 (L=4-[(2-hydroxyphenylimino)methyl]benzoic acid) containing poly(allylamine.HCl) polymer (PAlACuLbpy) as an electrocatalyst for oxygen reduction reaction (ORR). PAlACuLbpy was mixed with poly(acrylic acid) and tetraethylortho silicate to prepare a composite and then deposited on the screen printed electrode surface. The modified electrode (PAlACuLbpy/PCE) is highly stable and showed a quasi-reversible redox behavior with E 1 / 2 =-0.2 V vs. Ag/AgCl(3 M KCl) in 0.1 M phosphate buffer at pH 7 under argon atmosphere. PAlACuLbpy/PCE exhibited a remarkable ORR activity with an onset potential of-0.1 V vs Ag/AgCl in 0.1 M PB (pH 7) in the presence of oxygen. The kinetics for ORR was studied by rotating disk voltammetry in neutral aqueous medium and the results indicated that the number of electrons involving in the ORR is four and the conversion products are water and hydrogen peroxide.