Dielectric properties of polyethylene terephthalate/polyphenylene sulfide/barium titanate nanocomposite for application in electronic industry

Polymer/ceramic nanocomposites designed for application as electronic packaging were prepared using corotating twin‐screw extruder. The dielectric properties of the composites made from polyethylene terephthalate (PET), polyphenylene sulfide, and barium titanate were studied as a function of BaTiO₃ fraction in the range between 0.75 and 1.5 wt%. Processing parameters were optimized in order to obtain the nanocomposites with appropriate dielectric properties like dielectric permittivity ε′, dielectric losses ε″, and their temperature stability in a wide frequency range. The measurements showed the increase of the dielectric permittivity value ε′ in the composites in comparison to both pure polymers. The dielectric loss factor tgδ of the composites was found to be much smaller than that of the pure PET. The weak influence of the ceramics on the temperature stability of the dielectric properties of the composites was stated. POLYM. ENG. SCI., 50:1613–1619, 2010. © 2010 Society of Plastics Engineers     

Model for a Complex Analysis of Intelligent Built Environment

The purpose of intelligent built environment is to improve inhabitant's quality of life and to satisfy inhabitants by replacing routine work with smart devices and robots. Smart devices and robots can interpret changes in the built environment and respond appropriately. The problem is how to define a rational intelligent built environment when many various stakeholders are involved, projects have thousands of alternative versions and the quality of life and economical efficiency changes with alterations in micro and macro environmental conditions and the constituent parts of the process in question. Moreover, the realization of some objectives seems more rational from the economic perspective though their significance is varied from other perspectives. The formalized Model for Complex Analysis of Intelligent Built Environment and the Multiple Criteria Decision Support System of Intelligent Built Environment developed by the authors of this paper show how changes in project alternatives and the extent to which the goals of various stakeholders are satisfied cause respective changes in the value and utility degree of a project. To achieve the above-mentioned aims new multiple criteria analysis methods were developed.     

A free radical mechanism for inhibition of arteriosclerosis development with calcium antagonists

Work presents current views on involvement of free radicals in inhibition of development of arteriosclerosis by calcium antagonist (ACa). The importance of other substances, which interferes with calcium ions can contribute to the inhibition of arteriosclerosis development.     

Influence of Alkyl Chain Length on Thermal Properties,Structure, and Self-Diffusion Coefficients of Alkyltriethylammonium-Based Ionic Liquids

The application of ionic liquids (ILs) has grown enormously, from their use as simple solvents, catalysts, media in separation science, or electrolytes to that as task-specific, tunable molecular machines with appropriate properties. A thorough understanding of these properties and structure–property relationships is needed to fully exploit their potential, open new directions in IL-based research and, finally, properly implement the appropriate applications. In this work, we investigated the structure–properties relationships of a series of alkyltriethylammonium bis(trifluoromethanesulfonyl)imide [TEA-R][TFSI] ionic liquids in relation to their thermal behavior, structure organization, and self-diffusion coefficients in the bulk state using DSC, FT-IR, SAXS, and NMR diffusometry techniques. The phase transition temperatures were determined, indicating alkyl chain dependency. Fourier-transformed infrared spectroscopy studies revealed the structuration of the ionic liquids along with alkyl chain elongation. SAXS experiments clearly demonstrated the existence of polar/non-polar domains. The alkyl chain length influenced the expansion of the non-polar domains, leading to the expansion between cation heads in polar regions of the structured IL. ¹H NMR self-diffusion coefficients indicated that alkyl chain elongation generally caused the lowering of the self-diffusion coefficients. Moreover, we show that the diffusion of anions and cations of ILs is similar, even though they vary in their size.     

The effects of different UV‐B radiation intensities on morphological and biochemical characteristics in Ocimum basilicum L.

BACKGROUND: The effects of short‐term ultraviolet B (UV‐B) irradiation on sweet basil (Ocimum basilicum L. cv. Cinnamon) plants at the 3–4 leaf pair and flowering stages were examined in controlled environment growth chambers. Plants were exposed to 0 (reference), 2 and 4 kJ UV‐B m^?2 day^?1 over 7 days. RESULTS: Exposure of basil plants to supplementary UV‐B light resulted in increased assimilating leaf area, fresh biomass and dry biomass. Stimulation of physiological functions in young basil plants under either applied UV‐B dose resulted in increased total chlorophyll content but no marked variation in carotenoid content. At the flowering stage the chlorophyll and carotenoid contents of basil were affected by supplementary UV‐B radiation, decreasing with enhanced UV‐B exposure. Both total antioxidant activity (2,2‐diphenyl‐1‐picrylhydrazyl free radical assay) and total phenolic compound content were increased by UV‐B light supplementation. Young and mature basil plants differed in their ascorbic acid content, which was dependent on UV‐B dose and plant age. UV‐B radiation resulted in decreased nitrate content in young basil plants (3–4 leaf pair stage). CONCLUSION: These results indicate that the application of short‐exposure UV‐B radiation beneficially influenced both growth parameters and biochemical constituents in young and mature basil plants. © 2012 Society of Chemical Industry     

Correlated Dynamics in Ionic Liquids by Means of NMR Relaxometry: Butyltriethylammonium bis(Trifluoromethanesulfonyl)imide as an Example

¹H and ¹⁹F spin-lattice relaxation experiments have been performed for butyltriethylammonium bis(trifluoromethanesulfonyl)imide in the temperature range from 258 to 298 K and the frequency range from 10 kHz to 10 MHz. The results have thoroughly been analysed in terms of a relaxation model taking into account relaxation pathways associated with ¹H–¹H, ¹⁹F–¹⁹F and ¹H–¹⁹F dipole–dipole interactions, rendering relative translational diffusion coefficients for the pairs of ions: cation–cation, anion–anion and cation–anion, as well as the rotational correlation time of the cation. The relevance of the ¹H–¹⁹F relaxation contribution to the ¹H and ¹⁹F relaxation has been demonstrated. A comparison of the diffusion coefficients has revealed correlation effects in the relative cation–anion translational movement. It has also turned out that the translational movement of the anions is faster than of cations, especially at high temperatures. Moreover, the relative cation–cation diffusion coefficients have been compared with self-diffusion coefficients obtained by means of NMR (Nuclear Magnetic Resonance) gradient diffusometry. The comparison indicates correlation effects in the relative cation–cation translational dynamics—the effects become more pronounced with decreasing temperature.     

Relationship between Translational and Rotational Dynamics of Alkyltriethylammonium-Based Ionic Liquids

¹H spin-lattice relaxation experiments have been performed for a series of ionic liquids including bis(trifluoromethanesulfonyl)imide anion and cations of a varying alkyl chain length: triethylhexylammonium, triethyloctylammonium, decyltriethylammonium, dodecyltriethylammonium, triethyltetradecylammonium, and hexadecyltriethylammonium. The relaxation studies were carried out in abroad frequency range covering three orders of magnitude, from 10 kHz to 10 MHz, versus temperature. On the basis of a thorough, quantitative analysis of this reach data set, parameters characterizing the relative, cation-cation, translation diffusion (relative diffusion coefficients and translational correlation times), and rotational motion of the cation (rotational correlation times) were determined. Relationships between these quantities and their dependence on the alkyl chain length were discussed in comparison to analogous properties of molecular liquids. It was shown, among other findings, that the ratio between the translational and rotational correlation times is smaller than for molecular liquids and considerably dependent on temperature. Moreover, a comparison of relative and self-diffusion coefficients indicate correlated translational dynamics of the cations.     

Relative Cation-Anion Diffusion in Alkyltriethylammonium-Based Ionic Liquids

¹⁹F Nuclear Magnetic Resonance spin-lattice relaxation experiments have been performed for a series of ionic liquids including the same anion, bis(trifluoromethanesulfonyl)imide, and cations with alkyl chains of different lengths: triethylhexylammonium, triethyloctylammonium_, decyltriethylammonium, dodecyltriethylammonium, decyltriethylammonium, and hexadecyltriethylammonium. The experiments have been carried out in a frequency range of 10 kHz to 10 MHz versus temperature. A thorough analysis of the relaxation data has led to the determination of the cation–anion as a relative translation diffusion coefficient. The diffusion coefficients have been compared with the corresponding cation–cation and anion–anion diffusion coefficients, revealing a correlation in the relative translation movement of the anion and the triethylhexylammonium, triethyloctylammonium, decyltriethylammonium, and dodecyltriethylammonium cations, whereas the relative translation diffusion between the anion and the cations with the longer alkyl chains, decyltriethylammonium and hexadecyltriethylammonium, remains rather uncorrelated (correlated to a much lesser extent).     

Structural studies of poly(p-phenylene selenide) doped with sulphur trioxide

Poly(p-phenylene selenide) (PPSe) was prepared by condensation polymerization of 2,4 dibromobenzene and sodium selenide. The synthesis product in the form of powder was purified. The structure of the resulting polymer was investigated by infrared spectroscopy, wide-angle X-ray spectroscopy, electron diffraction, ultraviolet, electron spin resonance and elemental analysis.¹H-nuclear magnetic resonance (NMR) solid measurements were used to determine the molecular dynamics for undoped and SO₃-doped PPSe. The NMR investigations for undoped PPSe have shown that there are no essential differences in the structure and molecular motion between PPSe and PPS. After doping PPSe with SO₃, contrary to PPS, a third component of relaxation time,T ₁, is observed. The relaxation times for this component are connected to the interaction of protons with paramagnetic centres which are generated as a result of the doping process. The electrical conductivity of SO₃-doped PPSe at the beginning of the doping process rapidly increased to about 6 ×10^–6 S cm^–1 and then decreased more than one order of magnitude because of the chemical reaction which had occurred.