The effect of recycling number on the mechanical,chemical, thermal,and rheological properties of PBT/PC/ABS ternary blends: With and without glass‐fiber

The recycling possibilities of poly(butylene terephthalate)/polycarbonate/acrylonitrile–butadiene–styrene (PBT/PC/ABS) ternary blend with and without glass‐fiber content were investigated using repeated injection molding process. In this study, PBT/PC/ABS ternary blends were reprocessed at five times and the results were presented after each recycling process. The recycling possibility of PBT/PC/ABS ternary blend was evaluated by measuring the mechanical, chemical, thermal, and rheological properties. Mechanical properties were determined by the tensile strength, yield strength, strain at break, elastic modulus, impact strength, flexural strength, and flexural modulus. Chemical and thermal properties were evaluated by Fourier transform infrared spectroscopy, differential scanning calorimetry, thermal gravimetric analysis, and scanning electron microscopy. Rheological properties of the ternary blends were studied by melt flow index measurement. From the results, it was found that mechanical properties of recycled composites were better than virgin PBT/PC/ABS ternary blends. POLYM. COMPOS., 35:2074–2084, 2014. © 2014 Society of Plastics Engineers     

Hydrogen diffusivity enhancement in alumina pellets due to impregnated palladium

Single-pellet moment technique was used for the evaluation of effective diffusivities and adsorption equilibrium constants of hydrogen, carbon dioxide, and helium in pure alumina and palladium-impregnated alumina pellets. It was found that hydrogen was strongly adsorbed on palladium of Pd-alumina pellets, and significant enhancement of hydrogen diffusivity was observed due to impregnated palladium at 40°C. On the other hand, for carbon dioxide and helium, effective diffusivities obtained in Pd-alumina pellets were smaller than the corresponding values in pure alumina due to higher tortuosity factor values of Pd-alumina pellets.     

Petrochemicals from ethanol over a W-Si-based nanocomposite bidisperse solid acid catalyst

Very high ethylene selectivity values approaching 100% and very high ethanol conversion values approaching 85% were obtained in dehydration of ethanol over a new W-silicate-based nanocomposite catalyst having both meso and macropores and containing a W/Si atomic ratio of 0.85. Silicotungsticacid was successfully incorporated into the catalyst structure following a one-pot hydrothermal synthesis procedure. This catalyst is highly stable and does not loose activity in polar solvents and it has a sufficiently high surface area for catalytic applications. Calcination temperature of the catalyst was found to have a very significant effect on the catalyst structure and also on its catalytic performance in ethanol dehydration. Maximum selectivity of the second major reaction product diethylether was obtained as 0.7 at 200 °C, with the catalyst which was calcined at 400 °C. Very high ethylene and diethylether yield values obtained in this study at different reaction conditions are highly promising for the production of petrochemicals from ethanol.     

SMAQ: a measurement-based tool for traffic modeling and queuinganalysis. II. Network applications

For pt. I see ibid. p.56-65 (1998). SMAQ is a measurement-based tool for integration of traffic modeling and queuing analysis. It can be used in a variety of network design areas. For instance, it can be used as a traffic generator to generate various traces for network testing. It also provides numerical solutions of the queue length and loss rate performance for transport of multimedia traffic. Several application modules are built into the tool for the evaluation of statistical multiplexing, buffer dimensioning, and link bandwidth allocation. Other examples include the evaluation of traffic shaping, local-congestion control, and the modeling of wireless channel dynamics. As one will find, the SMAQ tool indeed provides a solution technique for network engineers to solve many of the current design issues     

Ultra-fast boriding of nickel aluminide

In this study, we explored the possibility of ultra-fast electrochemical boriding of nickel aluminide (Ni₃Al) in a molten borax electrolyte. Electrochemical boriding was performed at 950 °C for 15 min and at current densities ranging from 0.1 to 0.5 A/cm². The boride layers formed on the test samples were 50 to 260 μm thick depending on the current density. The mechanical, structural, and chemical characterization of the boride layers was carried out using a Vickers micro-hardness test machine, optical and scanning electron microscopes, and a thin film X-ray diffractometer. The hardness of boride layer was in the range from 800 to 1200 ± 50 HV depending on the load and the region from which the hardness measurements were taken. X-ray diffraction studies confirmed that the boride layers were primarily composed of Ni₃B, Ni₄B₃ and Ni₂₀AlB₁₄ phases. Structurally, the boride layer was very homogenous and uniformly thick across the borided surface area.     

Synthesis and characterization of V,Mo and Nb incorporated micro–mesoporous MCM-41 materials

Highly microporous metal-MCM-41 ordered mesoporous structure catalysts having different metal/Si (V, Mo, Nb) atomic ratios and combinations of metal sources were hydrothermally synthesized. The structural properties estimated using different techniques were found to be in agreement with each other. Metals were successfully incorporated into MCM-41 without deteriorating the ordered hexagonal structure. The metal ions in the synthesis solutions probably settled on the hydrophilic end of the template hence the metal incorporation resulted improvements in the micropore structure. Low loading of metals caused an increase in the surface area and pore volume values of the catalysts. The highest total (1310 m² g^?1) and micropore surface area values (1083 m² g^?1) were obtained by Nb incorporation. The micro- and mesopore dimensions of MCM-41 increased from 0.5 to 1.1 nm and from 2.5 to 2.8 nm, respectively, with metal incorporation. Low V/Si ratios and presence of Nb in the starting solution enhanced narrow mesopore size distribution. The pore dimension and wall thickness values estimated from nitrogen adsorption and X-ray diffraction methods were consistent with the corresponding values obtained using transmission electron microscopy.     

Chimeric ribonuclease as a source of human adapter protein for targeted drug delivery

Assembled modular complexes for targeted drug delivery can bebased on strong non-covalent interactions between a cargo modulecontaining an adapter protein and a docking tag fused to a targetingprotein. We have recently constructed a completely humanizedadapter/docking tag system based on interactions between 15amino acid (Hu-tag) and 110 amino acid (HuS) fragments of humanribonuclease I (RNase I). Although recombinant HuS can be expressedand refolded into a functionally active form, the purificationprocedure is cumbersome and expensive, and more importantly,it yields a significant proportion of improperly folded proteins.Here we describe engineering, high-yield expression, and purificationof a chimeric bovine/human RNase (BH-RNase) comprising 1–29N-terminal amino acids of bovine ribonuclease A and 30–127amino acids of human RNase I. Unlike RNase I, the chimeric BH-RNasecan be cleaved by either subtilisin or proteinase K betweenA20 and S21, providing a functionally active HuS. The HuS obtainedfrom chimeric BH-RNase differs from wild-type HuS by an N24Tsubstitution; therefore, we have reverted this substitutionby mutating N24 to T24 in BH-RNase. This BH-RNase mutant canalso be cleaved by subtilisin or proteinase K yielding wild-typeHuS. The affinity of HuS obtained from BH-RNase to Hu-tag isapproximately five times higher than that for recombinant HuS,reflecting a higher percentage of properly folded proteins. Received June 9, 2003; revised August 4, 2003; accepted August 28, 2003.     

Collapse of acrylamide‐based polyampholyte hydrogels in water

The swelling behavior of balanced acrylamide (AAm)‐based polyampholyte hydrogels in water and in aqueous salt (NaCl) solutions was investigated. Equimolar ratio of the ionic comonomers 4‐vinylpyridine (cationic monomer) and acrylic acid (anionic monomer) were used together with the nonionic monomer AAm in the hydrogel preparation. The variations of the hydrogel volume in response to changes in pH were measured. It was found that the hydrogels are in a collapsed state not only at the pH of the isoelectric point pH_IEP but also over a wide range of pH including pH_IEP. The width of the collapsed plateau increased and the hydrogels assumed a more compact state as the ionic group content is increased. The antipolyelectrolyte behavior was observed along the collapsed plateau region, where the gel occupies a larger volume in salt solution. The experimental swelling data were compared with the predictions of the Flory‐Rehner theory of swelling equilibrium including the ideal Donnan equilibria. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009