High-performance polymer alloys of polybenzoxazine and bismaleimide

Two series of high-performance polymer alloys were prepared by mixing typical benzoxine monomers, 3-phenyl-3,4-dihydro-2H-1,3-benzoxazine (P-a) or 6,6-(1-methylethyliden)-bis-(3,4-dihydro-3-phenyl-2H-1,3-benzoxazine) (B-a), with a typical bismaleimide, 4,4-bismaleimidodiphenyl methane by various ratios followed by thermal treatment up to 240 °C. DSC and IR of the alloys were examined to follow the curing reaction. These analyses showed that the obtained polymer alloys are AB co-cross-linked polymer networks through the formation of ether linkage between the hydroxyl group of polybenoxazine and the double bond of bismaleimide. Viscoelastic analysis and softening temperature measurement revealed that the polymer alloys have much higher glass transition temperatures than those of each homopolymer. The thermal stability also increased with the increase of bismaleimide content as evidenced by TGA.     

Novel thermally and mechanically stable hydrogel for enzyme immobilization of penicillin G acylase via covalent technique

κ‐Carrageenan hydrogel crosslinked with protonated polyethyleneimine (PEI⁺) and glutaraldehyde (GA) was prepared and evaluated as a novel biocatalytic support for covalent immobilization of penicillin G acylase (PGA). The method of modification of the carrageenan biopolymer is clearly illustrated using a schematic diagram and was verified by FTIR, elemental analysis, DSC, and INSTRON using the compression mode. Results showed that the gels' mechanical strength was greatly enhanced from 3.9 kg/cm² to 16.8 kg/cm² with an outstanding improvement in the gels thermal stability. It was proven that, the control gels were completely dissolved at 35°C, whereas the modified gels remained intact at 90°C. The DSC thermogram revealed a shift in the endothermic band of water from 62 to 93°C showing more gel‐crosslinking. FTIR revealed the presence of the new functionality, aldehydic carbonyl group, at 1710 cm^?1 for covalent PGA immobilization. PGA was successfully immobilized as a model industrial enzyme retaining 71% of its activity. The enzyme loading increased from 2.2 U/g (control gel) to 10 U/g using the covalent technique. The operational stability showed no loss of activity after 20 cycles. The present support could be a good candidate for the immobilization of industrial enzymes rich in amino groups, especially the thermophilic ones. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Anaerobic biodegradability and treatment of grey water in upflow anaerobic sludge blanket (UASB) reactor

Feasibility of grey water treatment in an upflow anaerobic sludge blanket (UASB) reactor operated at different hydraulic retention time (HRT) of 16, 10 and 6h and controlled temperature of 30 degrees C was investigated. Moreover, the maximum anaerobic biodegradability without inoculum addition and maximum removal of chemical oxygen demand (COD) fractions in grey water were determined in batch experiments. High values of maximum anaerobic biodegradability (76%) and maximum COD removal in the UASB reactor (84%) were achieved. The results showed that the colloidal COD had the highest maximum anaerobic biodegradability (86%) and the suspended and dissolved COD had similar maximum anaerobic biodegradability of 70%. Furthermore, the results of the UASB reactor demonstrated that a total COD removal of 52-64% was obtained at HRT between 6 and 16 h. The UASB reactor removed 22-30% and 15-21% of total nitrogen and total phosphorous in the grey water, respectively, mainly due to the removal of particulate nutrients. The characteristics of the sludge in the UASB reactor confirmed that the reactor had a stable performance. The minimum sludge residence time and the maximum specific methanogenic activity of the sludge ranged between 27 and 93 days and 0.18 and 0.28 kg COD/(kg VS d).     

A new taxonomy of routing algorithms for wireless mobile ad hoc networks: the component approach

Over the past decade, wireless multihop ad hoc networks have received a tremendous amount of research focus, at the core of which lies the design problem for efficient routing algorithms to meet various scenarios and applications. The axiom, "one size doesn't fit all," continues to stand firmly to this day. In light of this, we introduce a new routing design concept - the component approach. We examine existing routing protocols and break them down into smaller building blocks, namely, routing components. The component analysis and classification results show that most routing protocols can be functionally decomposed into several basic routing components. This fact indicates that it is feasible to design a component-based routing (CBR) protocol. With a different realization for each basic routing component, it is expected that the routing behavior of CBR can be tailored to different application profiles and time-varying environment parameters at a reasonable cost     

Photocatalytic oxidation of ciprofloxacin under simulated sunlight

Ciprofloxacin (CIP) is a famous synthetic chemotherapeutic antibiotic. It is widely found either in water or wastewater. In this study ciprofloxacin was photocatalytically degraded using commercial anatase titanium dioxide (TiO(2)) under simulated sunlight. The rate of reaction was found to be affected by pH, TiO(2) concentration and antibiotic concentration. The best reaction rate was obtained in natural ciprofloxacin pH (5.8) and 1000 mg/L TiO(2). More titania concentration was found to reduce the reaction rate because of the limitation in light transmittance. From kinetic studies, the reaction was proved to proceed through adsorption step then photooxidation and obeys pseudo-first order kinetics.     

Copper cation removal in an electrokinetic cell containing zeolite

Zeolites are used in environmental remediation of soil or water to immobilize or remove toxic materials by cation exchange. An experiment was conducted to test the use a low electric field to direct the toxic cations towards the zeolite. An electrokinetic cell was constructed using carbon electrodes. Synthetic Linde Type A (LTA) zeolite was placed in the cell. Copper(II) chloride dissolved in water was used as a contaminant. The Cu(2+) concentration was measured for ten hours with and without an applied electric field. The removal of the Cu(2+) ions was accelerated by the applied field in the first two hours. For longer time, the electric field did not improve the removal rate of the Cu(2+) ions. The presence of zeolite and applied electric field complicates the chemistry near the cathode and causes precipitation of Cu(2+) ions as copper oxide on the surface of the zeolite. With increased electric field the zeolite farther away from the cathode had little cation exchange due to the higher drift velocity of the Cu(2+) ions. The results also show that, in the LTA Zeolite A pellets, the cation exchange of Cu is limited to a shell of several tens of micrometers.     

Stoffaustausch zwischen flüssigem Eisen und Schlacke beim Sprühraffinationsverfahren

Erläuterung des Sprühraffinationsverfahrens, bei dem eine Schmelze mit inertem Gas verdüst wird und die entstehenden Metalltropfen durch eine Raffinationsschlacke fallen. Erörterung der Gesetzmäßigkeiten für die Stoffaustauschvorgänge zwischen Metalltropfen und Schlacke. Bestimmung der mittleren Tropfengröße beim Versprühen von kohlenstoffgesättigtem Roheisen. Untersuchung der Wirkung der Sprühraffination am Beispiel der Entschwefelung des Roheisens mit Schlacken des Systems CaO–CaF₂–Al₂O₃ bei 1600 °C. Ermittlung des Stoffübergangskoeffizienten des Schwefels für den umgekehrt transitorischen Phasenkontakt und Vergleich mit Werten bei anderen Techniken des Phasenkontaktes Metall-Schlacke.