Suitability Of Preparation Research Articles

Morphological, structural, dielectric and electrical properties of PEO–ZnO nanodielectric films

The morphological, structural, dielectric and electrical properties of aqueous solution-cast prepared poly(ethylene oxide)–zinc oxide (PEO–ZnO) nanocomposite films have been investigated as a function of ZnO nanoparticle concentrations up to 5 wt%. Scanning electron microscopy (SEM) images of these films show that the morphology of pristine PEO aggregated spherulites changes into fluffy, voluminous and highly porous with dispersion of ZnO nanoparticles into the PEO matrix. X-ray diffraction (XRD) study confirms that the crystalline phase of PEO greatly reduces at 1 wt% ZnO, and it again increases gradually with further increase of ZnO concentration. The dielectric relaxation spectroscopy (DRS) over the frequency range 20 Hz–1 MHz reveals that the real part of complex dielectric permittivity at audio frequencies decreases non-linearly whereas it remains almost constant at radio frequencies for these polymeric nanocomposites. Dispersion of nanosize ZnO particles into the PEO matrix reduces the values of dielectric permittivity which also exhibits a correlation with the dispersivity of ZnO nanoparticles. The relaxation peaks observed in the dielectric loss tangent and electric modulus spectra reveal that the electrostatic interactions of nanoscale ZnO particles with the ethylene oxide functional dipolar group of PEO monomer units decrease the local chain segmental dynamics of the polymer. Real part of ac conductivity spectra of these films have been analyzed by power law fit over the audio and radio frequency regions, respectively, and the obtained dc conductivity values for these regions differ by more than two orders of magnitude. The temperature dependent relaxation time and dc conductivity values of the nanodielectric material obey the Arrhenius relation of activation energies and confirm a correlation between dc conductivity and PEO chain segmental motion which is exactly identical to the characteristics of solid polymer electrolytes. Results imply that these nanocomposite materials can serve as low permittivity flexible nanodielectric for radio frequency microelectronic devices and also as electrical insulator for audio frequency operating conventional devices in addition to their suitability in preparation of solid polymer electrolytes.

Structural characterization of hydrophilic polymer blends/montmorillonite clay nanocomposites

ABSTRACTThe nanocomposite films comprising polymer blends of poly(vinyl alcohol) (PVA), poly(vinyl pyrrolidone) (PVP), poly(ethylene oxide) (PEO), and poly(ethylene glycol) (PEG) with montmorillonite (MMT) clay as nanofiller were prepared by aqueous solution casting method. The X‐ray diffraction studies of the PVA–x wt % MMT, (PVA–PVP)–x wt % MMT, (PVA–PEO)–x wt % MMT and (PVA–PEG)–x wt % MMT nanocomposites containing MMT concentrations x = 1, 2, 3, 5 and 10 wt % of the polymer weight were carried out in the angular range (2θ) of 3.8–30°. The values of MMT basal spacing d001, expansion of clay gallery width Wcg, d‐spacing of polymer spherulite, crystallite size L and diffraction peak intensity I were determined for these nanocomposites. The values of structural parameters reveal that the linear chain PEO and PEG in the PVA blend based nanocomposites promote the amount of MMT intercalated structures, and these structures are found relatively higher for the (PVA–PEO)–x wt % MMT nanocomposites. It is observed that the presence of bulky ester‐side group in PVP backbone restricts its intercalation, whereas the adsorption behavior of PVP on the MMT nanosheets mainly results the MMT exfoliated structures in the (PVA–PVP)–x wt % MMT nanocomposites. The crystallinities of the PEO and PEG were found low due to their blending with PVA, which further decreased anomalously with the increase of MMT concentration in the nanocomposites. The decrease of polymer crystalline phase of these materials confirmed their suitability in preparation of novel solid polymer nanocomposite electrolytes. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014, 131, 40617.

Scanning Probe Microscopy Method for Nanosuspension Stabilizer Selection

An atomic force microscopy (AFM) method was successfully developed and utilized for investigating the interaction of polymeric stabilizers with ibuprofen to determine their suitability for the preparation and stabilization of ibuprofen nanosuspensions. Images obtained clearly showed that HPMC and HPC interacted strongly with the ibuprofen resulting in extensive surface adsorption, confirming their suitability for ibuprofen nanosuspension preparation. In addition, differences in the morphology of the adsorbed HPMC and HPC molecules were observed, which may be attributed to their variable degree of substitution. Consistent with their poor performance in stabilizing the ibuprofen nanosuspensions, images obtained with PVP and Poloxamer's depicted inadequate adsorption on the ibuprofen surface. Careful analysis of the AFM images and the ibuprofen crystal structure gave valuable insight into the success of top-down processing for the preparation of nanosuspensions as compared to bottom-up processing. On the basis of the relationship observed between nanosuspension stability and adsorption characteristics of specific polymers, such AFM studies can aid in the selection of suitable nanosuspension stabilizers. This method provides the basis for a scientific rationale for nanosuspension stabilizer selection rather than the trial and error method which is currently practiced.

Evaluation of polyester, epoxy and acrylic resins for suitability in preparation of soil thin sections for in situ biological studies

Micromorphological investigations which aim to integrate both physical and biological features of soils are particularly demanding with respect to the quality of the thin sections produced for such studies. Rapid preparation of thin sections is also often desirable. The suitability of a range of resins for the rapid preparation of high-quality thin sections appropriate for biologically oriented studies was tested. Preparative procedures were investigated using four undisturbed soils (albic, calcic, humic, and argillic horizons) chosen to exhibit contrasting properties. Roots of sown Lolium perenne, their associated AM-mycorrhizas, and indigenous fungi and actinomycetes of the soils were used as indicators of the quality of preservation of biological material in sections of 15 μm thickness. Crystic 17449 and Palatal P50-01 proved most suitable, producing durable sections in 2–3 weeks with excellent preservation of roots, microbes and inorganic features in all the soils tested.