Nonisothermal melt-crystallization kinetics of isotactic polypropylene synthesized with a metallocene catalyst and compounded with different quantities of an α nucleator

The nonisothermal crystallization kinetics of a metallocene-made isotactic polypropylene (m-iPP) and its compounds with 0.1 wt % and 0.3 wt % of a sorbitol derivative [1,3:2,4-bis(3,4-dimethylbenzylidene)sorbitol (DMDBS); an α nucleator] were investigated by differential scanning calorimetry at different cooling rates from the melt. The nucleation efficiency was proved by a significant increase in the crystallization temperatures (accompanied by a slight augmentation of the degree of crystallinity and a decrease in the crystal sizes). This increase in the crystallization temperatures led to higher amounts of fractional content in the γ polymorph, even though DMDBS was supposed to be a nucleator for the α form. The Avrami and Ozawa methods effectively described only the early stage of crystallization, whereas a combined Avrami–Ozawa method was valid for the whole crystallization process. The values of the exponent for this method decreased for nucleated samples in the later stage of crystallization, especially in the case of m-iPP with 0.3 wt % DMDBS added (m-iPP03). The activation energy of the process and the surface free energy were also estimated. The production of considerable proportions of the γ polymorph in m-iPP03 corresponded to higher values of the activation energy and lower values of the surface free energy. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Computer simulation of the effective double layer occurring on a catalyst surface under electro-chemical promotion conditions

In this work, the structural and energetic properties of two typical catalytic surfaces, Na/Pt(111) and O/Pt(111), are studied by means of quantum mechanical calculations and Monte Carlo Grand Canonical simulations. The simulations were performed with electrostatic potentials at different truncation schemes. In order to elucidate the modification of catalyst surfaces produced by the backspillover of ionic species onto Pt(111), the electrostatic field at the interface due to the electric double layer was also analyzed.     

Time and temperature effect on the linear–nonlinear viscoelastic transition threshold of a polymeric system

In the present study, the transition of a polymeric material from the linear to the nonlinear viscoelastic behavior and the determination of the nonlinearity stress threshold variation with time and temperature are investigated. For this purpose a systematic experimental program consisted of thermal and mechanical characterization of certain polymeric material followed by isothermal creep tests at different stress levels and temperatures was conducted. Through isochronal curves that occurred from creep tests, the nonlinearity threshold dependence on both time and temperature is presented. The reported results provide information that is critical for the design and development of polymer structures and components. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Dispersion characterization in layered double hydroxide/Nylon 66 nanocomposites using FIB imaging

Layered double hydroxides (LDHs), a newly emerging 2D host material, consist of cationic brucite-like layers and exchangeable interlayer anions. In this work, the morphology and dispersion of LDH particles in LDH/Nylon 66 (salt) nanocomposites has been investigated using focused ion beam (FIB) techniques, transmission electron microscopy (TEM) and X-ray diffraction (XRD). The FIB images show that LDHs are present in the polymer phase dispersed to different degrees, with partial intercalation, exfoliation, and aggregation all being observed. The most even dispersion was achieved in nanocomposites with the lowest loading (0.5 wt % LDH). Residual tactoids and agglomerates were most common in the samples made with the highest concentration of LDHs studied here (5 wt %). The dispersion observed using FIB was consistent with TEM and XRD analysis, yet this technique had significant benefits in terms of time and simplicity over these “conventional” technologies. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Dual band-notched ultra-wideband microstrip antenna using asymmetrical spurlines

A simple and novel ultra-wideband microstrip-fed antenna with dual band-notched characteristic is presented. By etching a pair of asymmetrical spurlines on the feedline, two notched bands of 600 MHz (3.95? 4.55 GHz) and 650 MHz (5.35?6.0 GHz) are achieved. Measured results show that this antenna operates from 2.5 to 12.0 GHz for voltage standing wave ratio less than 2, except two frequency notched bands of 3.95?4.55 GHz and 5.35?6.0 GHz. Moreover, this antenna has good omnidirectional radiation patterns in the H-plane.     

Switching Device Based on a Thin Film of an Azo-Containing Polymer for Application in Memory Cells

Results obtained on a conductive multilevel device realized with a 100 nm azo-polymer film are reported. The capability to switch between three different conductance states makes the device versatile both for Write Once Read Many and Write Many Read Many memory cell application. The analysis of the - curves indicates that the hysteretic conductance change with the external voltage can be explained in terms of different hopping distances existing between the nearest neighbors intervening in the two conformational states of the molecular structure.     

Nonequilibrium nonstoichiometry in ionic compounds

Ionic substances under normal conditions are stoichiometric compounds with phase diagrams featuring no homogeneity regions. Crystals grown under nonequilibrium conditions, in particular, under significant centrifugal acceleration, are characterized by nonstoichiometric compositions (e.g., K_2−x Br_1.07). In this way, it is possible to obtain nonequilibrium nonstoichiometric ionic compounds possessing certain homogeneity regions. Nonstoichiometric crystals of KCl, KBr, and KI grown under various accelerations ranging within (1.3–100.0)×10³ g exhibit insignificant variations in the lattice constants and a significant increase in micro-hardness with acceleration.     

Chaotic Homogeneous Porous Media. 3. Basic Parameters of Macrodispersion

The basic notions and parameters of a macrodispersion continuum — inner and outer scales, intensity, hydraulic resistance, and thermal resistance — are presented and analyzed. The notion of a macrodispersion shell has been specified and the Darcy law has been refined.     

Mechanochemical modification of the phase diagrams of hexagonal oxide ferrimagnets

Mechanical activation and fine comminution of hexagonal oxide ferrimagnets by milling to a nanocrystalline state (ultradisperse powder), followed by sintering, leads to significant changes in the phase diagram, the temperature of synthesis, and the magnetic properties as compared to those of the materials obtained by traditional ceramic technology. The final material structure is formed through “chemical assembly”—sequential consolidation of nanodimensional particles (structure-forming blocks)—rather than through the formation of low-temperature phases and their decomposition with increasing temperature.     

Biodegradation of phenol at low temperature using two-phase partitioning bioreactors.

Two-phase partitioning bioreactors offer many advantages for the removal of toxic pollutants. In particular, such systems can be loaded with very large quantities of pollutants without risks of microbial inhibition, they are self-regulated and they prevent the risks of hazardous pollutant volatilisation during aerobic treatment. However, their potential has never been tested at low temperatures. Phenol biodegradation by a cold adapted Pseudomonas strain was therefore tested at 14 or 4 degrees C using 2-undecanone, diethyl sebacate or 2-decanone as organic phases in a two-phase partitioning bioreactor. The three solvents were biocompatible at 14 degrees C but evidence was found that diethyl sebacate was biodegraded by the bacteria and this solvent was not tested further. Although only 2-decanone was suitable at 4 degrees C, phenol biodegradation was more efficient in 2-undecanone at 14 degrees C, reaching a maximum volumetric rate (based on the volume of aqueous phase) of approximately 1.94 g/L.day after 47 h of cultivation. In 2-decanone at 14 degrees C, evidence was found that phenol degradation was limited by the release of biosurfactants, which increased the solubility and toxicity of the solvent in the aqueous phase inhibiting microbial activity. This study therefore shows that pollutant removal at low temperature is feasible but that the production of biosurfactants can have a negative impact on the process and must be taken into consideration when selecting the organic solvent. Future work should therefore focus on the selection of solvents suitable for use at temperatures below 14 degrees C.