This is a report on photo-irradiated extracellular synthesis of silver nanoparticles using the aqueous extract of edible oyster mushroom (Pleurotus florida) as a reducing agent. The appearance, size, and shape of the silver nanoparticles are understood by UV-visible spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, and atomic force microscopy. The X-ray diffraction studies, energy dispersive X-ray analysis indicate that particles are crystalline in nature. Fourier transform infrared spectroscopy analysis revealed that the nanoparticles are covered with biomoieties on their surface. As can be seen from our studies, the biofunctionalized silver nanoparticles thus produced have shown admirable antimicrobial effects, and the synthetic procedure involved is eco-friendly and simple, and hence high range production of the same can be considered for using them in many pharmaceutical applications.

Using reactors of different sizes and geometries the dynamics of the frontal polymerization of 1,6-hexanediol diacrylate (HDDA) and pentaerythritol tetraacrylate (PETAC), with ammonium persulfate as the initiator were studied. For this system, the frontal polymerization exhibits complex behavior that depends on the ratio of the monomers. For a particular range of monomers concentration, the polymerization front becomes nonplanar, and spin modes appear. By varying the reactor diameter, we experimentally confirmed the expected shift of the system to a greater number of "hot spots" for larger diameters. For square test tubes a "zig-zag" mode was observed for the first time in frontal polymerization. We confirmed the viscosity-dependence of the spin mode instabilities. We also observed novel modes in cylinder-inside-cylinder reactors. Lastly, using a conical reactor with a continuously varying diameter, we observed what may be evidence for bistability depending on the direction of propagation. We discuss these finding in terms of the standard linear stability analysis for propagating fronts. (c) 2002 American Institute of Physics.

Conducting polyaniline-polymannuronate (PANI-PM) composites were synthesized via in situ deposition techniques. By dissolving different weight percentages of polymannuronate (PM) (5, 10, 15, and 25%), the oxidative polymerization of aniline was achieved through the use of ammonium persulfate as oxidant. Structural morphology, FT-IR, and X-ray diffraction (XRD) studies support a strong interaction between PANI and PM. The temperature-dependent DC conductivity of PANI-PM composites was studied within the range of 300 T 500 K, presenting evidence for the transport properties of PANI-PM composites. Conductivity was analyzed through Mott's equation, which leveraged the variable range hopping model in three dimensions. Parameters such as density of states at the Fermi energy, hopping energy, and hopping distance were calculated. Based on the above factors, the synthesis of PANI-PM composites envisages the future development of biomimetic materials for the creation of a new bionanocomposite as a multicomponent and multifunctional material.

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