Strain-Free Total Resonant Sextet Benzenoid Hydrocarbons

The importance of strain-free (total) resonant sextet benzenoid hydrocarbons is pointed out. The first computer-aided generation and enumeration of such systems is reported, and the data represent substantial supplements to the previous numbers of strain-free resonant sextet benzenoid isomers. Supplementary depictions of some forms of the systems in question are also provided. Constant-isomer series are delineated for the resonant sextet benzenoids. The numbers associated with these series are found to match exactly the known numbers for corresponding constant-isomer series of strictly pericondensed benzenoids.     

Influence of processing on morphology in short aramid fiber reinforced elastomer compounds

The rubber industry is nowadays facing the general increase of raw materials as the customers are confronted with rising prices for energy. Therefore there is a need for higher durability of elastomer applications. Short fiber reinforced elastomers can contribute to the improvement of dynamic and wear properties. To determine structure–property relationships in short fiber reinforced elastomer compounds it is of crucial interest to know the contributions of fiber aspect ratio, volume content, orientation and fiber–elastomer interaction. Therefore the influence of different processing conditions and fiber contents on the resulting morphology and macroscopic properties was investigated in this article by the help of fluorescence and confocal laser microscopy using a transparent ethylene‐propylene‐diene rubber (EPDM) matrix. It was found that the processing induced fiber breakage was the key factor in determining the composite morphology and subsequent physical properties. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1682–1690, 2013     

COD and AOX Removal and Biodegradability Assessment for Fenton and O3/UV Oxidation Processes: A Case Study from a Graphical Industry Wastewater

Due to process stability and excellent effluent quality, the use of membrane processes is rapidly expanding. However, a drawback is the production of concentrates and their proper disposal. In this study, reverse osmosis concentrate was treated by Fenton and O₃/UV oxidation processes. The concentrate contains halogenated compounds, recalcitrant COD and low biodegradability. The removal of halogenated compounds and the enhancement of biodegradability were examined. Comparing the investigated processes, Fenton oxidation resulted in a better mineralization of organic matter; however, O₃/UV oxidation achieved a better enhancement of the biodegradability. Furthermore, similar degradation of halogenated compounds were observed for both oxidation processes.     

Influence of shear flow on the preparation of polymer layered silicate nanocomposites

In this paper the influence of melt-processing on the final polymer/layered silicate nanocomposite morphology is discussed. In particular the role of shear forces on the transformation of the original large clay agglomerates is of interest. Several polymer nanocomposites were prepared by melt-extrusion, involving polycaprolactone, poly(ethylene oxide), polyamide-12 or polyamide-6 as the matrix polymer. The nanocomposite morphology was characterised by X-ray diffraction and transmission electron microscopy and the clay tactoid morphology with polarised optical microscopy and scanning electron microscopy. The development of the tactoid and nanocomposite morphology during melt-mixing under shear was studied time-resolved by optical microscopy in conjunction with a rheometer and synchrotron X-ray scattering together with a Couette type flow cell. The shear forces in the melt-preparation of polymer layered mineral nanocomposites facilitate the break-up of large-sized agglomerates, whereas the extent of further exfoliation of the mineral layers is determined by the compatibility between the polymer matrix and the mineral layers rather than by shear forces.     

Effect of grass vs. concentrate feeding on the fatty acid profile of different fat depots in lambs

The aim of this study was to produce high‐quality meat from lambs under different feeding conditions, as measured by the accumulation of n‐3 fatty acids and conjugated linoleic acids (CLA) in muscle and subcutaneous fat. In total, 13 male crossbred lambs (Black Head×Gotland), each at 24 kg live weight, were divided into two feeding groups. Lambs were kept either on pasture (pasture grazing, n = 6) or in the stable (concentrate feeding, n = 7). The linolenic acid (C18:3n‐3) contained in the grass was absorbed and deposited into the different lipid classes of muscle and subcutaneous fat. The proportion of total n‐3 fatty acids in the different lipids of grazing lambs was significantly (p = 0.05) higher compared to that in concentrate‐fed lambs. The n‐6/n‐3 ratio (mean ± SEM) in muscle of grazing lambs was 1.2 ± 0.09 in contrast to 2.3 ± 0.09 (p = 0.05) of the animals kept in the stable. In subcutaneous fat, this ratio was 0.9 ± 0.2 in lambs kept on pasture versus 3.5 ± 0.2 (p = 0.05) after indoor keeping. The relative concentration of C18:1trans‐11 in total muscle lipids, phospholipids, triacylglycerols and subcutaneous fat was significantly increased by grass feeding compared to concentrate feeding. Significant influences of feeding were shown for saturated fatty acids. In concentrate‐fed lambs, a lower content of saturated fatty acids was detected. The proportion of CLAcis‐9,trans‐11 (1.9 ± 0.2% vs. 1.1 ± 0.1% in muscle, 2.5 ± 0.2% vs. 1.4 ± 0.2% in subcutaneous fat, 0.7 ± 0.04% vs. 0.4 ± 0.04% in phospholipids) in lambs was significantly (p = 0.05) higher after grazing than after concentrate feeding, respectively.     

Reduction of NOx by H2 on WOx-Promoted Pt/Al2O3/SiO2 Catalysts Under O2-Rich Conditions

This work addresses the reduction of NO_x by H₂ under O₂-rich conditions using Al₂O₃/SiO₂-supported Pt catalysts with different loads of WO_x promotor. The samples were thoroughly characterised by N₂ physisorption, temperature-programmed desorption of CO, scanning electron microscopy, X-ray diffraction, laser raman spectroscopy, X-ray photoelectron spectroscopy and diffuse reflectance infrared fourier transform spectroscopy with probe molecule CO. The catalytic studies of the samples without WO_x showed pronounced NO_x conversion below 200 °C, whereas highest efficiency was related to small Pt particles. The introduction of WO_x provided increasing deNO_x activity as well as N₂ selectivity. This promoting effect was referred to an additional reaction path at the Pt-WO_x/Al₂O₃/SiO₂ interface, whereas an electronic activation of Pt by strong metal support interaction was excluded.

Graphic Abstract

     

Borcalein: a Carborane-Based Analogue of Baicalein with 12-Lipoxygenase-Independent Toxicity

12-Lipoxygenase is crucial for tumour angiogenesis. 5,6,7-Trihydroxy-2-phenyl-4H-1-benzopyran-4-one (baicalein) is a suitable inhibitor for this enzyme but is rapidly metabolised in vivo. Thus, an improvement of the metabolic stability is necessary to enhance the therapeutic efficiency. An emerging approach to enhance metabolic stability of carbon-based pharmaceuticals is the use of metabolically stable, non-toxic boron clusters, such as dicarba-closo-dodecaborane(12)s (carboranes) as phenyl mimetics. Therefore, the unsubstituted phenyl ring of baicalein was replaced by meta-carborane, resulting in borcalein, the carborane analogue of baicalein. This substitution resulted in a decreased inhibitory activity toward 12-lipoxygenase, but led to increased toxicity in melanoma (A375, B16, B16F10) and colon cancer cell lines (SW480, HCT116, CT26CL25) with decreased tumour selectivity in comparison to baicalein. Surprisingly, borcalein displays a different mechanism of cytotoxicity with increased intracellular production of reactive oxygen species (ROS), reactive nitrogen species (RNS) and nitric oxide (NO).     

Structure-Activity Relationships for 5′′ Modifications of 4,5-Aminoglycoside Antibiotics

Modification at the 5’’-position of 4,5-disubstituted aminoglycoside antibiotics (AGAs) to circumvent inactivation by aminoglycoside modifying enzymes (AMEs) is well known. Such modifications, however, unpredictably impact activity and affect target selectivity thereby hindering drug development. A survey of 5’’-modifications of the 4,5-AGAs and the related 5-O-furanosyl apramycin derivatives is presented. In the neomycin and the apralog series, all modifications were well-tolerated, but other 4,5-AGAs require a hydrogen bonding group at the 5’’-position for maintenance of antibacterial activity. The 5’’-amino modification resulted in parent-like activity, but reduced selectivity against the human cytosolic decoding A site rendering this modification unfavorable in paromomycin, propylamycin, and ribostamycin. Installation of a 5’’-formamido group and, to a lesser degree, a 5’’-ureido group resulted in parent-like activity without loss of selectivity. These lessons will aid the design of next-generation AGAs capable of circumventing AME action while maintaining high antibacterial activity and target selectivity.     

Influence of Stress and Chemical Homogeneity on Dielectric Properties of BaTi0.9Zr0.1O3

The influence of mechanical stress and chemical homogeneity on the permittivity of BaTi_0.9Zr_0.1O₃ ceramics prepared from mixed-oxide and hydrothermal powders was studied. To reduce stress, liquid-phase sintering was applied in conjunction with a low heating rate to stimulate the formation of large grains. The influence of chemical homogeneity was studied by variations in sintering temperatures and times. For both types of ceramics, the dielectric constant at the Curie temperature was influenced by both factors, but to a different extent. In the mixed oxide ceramic, chemical homogeneity played a more prominent role, while internal stress appeared to exert a larger influence in the hydrothermal ceramics. The dielectric constant at the Curie temperature could be increased by 5%–10% by an annealing treatment at 200°C, followed by slow cooling.