A solid phase extraction procedure for Fe3+, Cu2+ and Zn2+ ions on 2-phenyl-1H-benzo[d] imidazole loaded on Triton X-100-coated polyvinyl chloride

A new and efficient solid phase extraction method is described for the preconcentration of trace heavy metal ions. The method is based on the adsorption of Fe(3+), Cu(2+) and Zn(2+) on 2-phenyl-1H-benzo[d] imidazole (PHBI) loaded on Triton X-100-coated polyvinyl chloride (PVC). The influences of the analytical parameters including pH and sample volume were investigated. Common coexisting ions did not interfere on the separation and determination of analytes under study. The adsorbed analytes were desorbed by using 5 mL of 4 mol L(-1) nitric acid. The preconcentration factor is 90. The detection limits (3 sigma) were in the range of 0.95-1 microg L(-1). The sorbent exhibited excellent stability and its sorption capacity under optimum conditions has been found to be more than 2.7 mg of ions per gram of sorbent. The recoveries of analytes were generally higher than 95%. The relative standard deviations (R.S.D.s) were generally lower than 4%. The method has been successfully applied to some real samples.     

Cellular uptake, cytotoxicity, and metabolic profiling of human cancer cells treated with ruthenium(II) polypyridyl complexes [Ru(bpy)2(N--N)]Cl2 with N--N=bpy, phen, dpq, dppz, and dppn

A series of five ruthenium(II) polypyridyl complexes [Ru(bpy)2(N--N)]Cl2 was tested against human HT-29 and MCF-7 cancer cell lines. Cellular uptake efficiency and cytotoxicity were found to increase with the size of the aromatic surface area of the N--N ligand. The most active compound carrying the dppn ligand exhibits a low micromolar IC(50) value against both cell lines comparable to that of cisplatin under similar conditions. Continuous measurement of oxygen consumption, extracellular acidification rate, and impedance of the cell layer with a chip-based sensor system upon exposure to the complexes showed only small changes for the first two parameters throughout the series. A significant and irreversible decrease in impedance was, however, found for the dppn compound. This suggests that its biological activity is related to modifications in cell morphology or cell-cell and cell-matrix contacts.     

Failure analysis of a second stage blade in a gas turbine engine

The failure of a second stage blade in a gas turbine was investigated by metallurgical and mechanical examinations of the failed blade. The blade was made of a nickel-base alloy Inconel 738LC. The turbine engine has been in service for about 73,500 h before the blade failure at 5:50 PM on 14 August 2004. Due to the blade failure, the turbine engine was damaged severely. The investigation was started with a thorough visual inspection of the turbine and the blades surfaces, followed by the fractography of the fracture surfaces, microstructural investigations, chemical analysis and hardness measurement.

The observation showed that a serious pitting was occurred on the blade surfaces and there were evidences of fatigue marks in the fracture surface. The microstructural changes were not critical. It was found that the crack initiated by the hot corrosion from the leading edge and propagated by fatigue and finally, as a result of the reduction in cross-section area, fracture was completed.

An analytical calculation parallel to the finite element method was utilized to determine the static stresses due to huge centrifugal force. The dynamic characteristics of the turbine blade were evaluated by the finite element modal and harmonic analyses. Finally according to the log sheet records and by using a Campbell diagram there was a good agreement between the failure signs and FEM results which showed the broken blade has been resonated by the third vibrational mode occasionally before the failure occurred.     

Electrokinetically synchronized polymerase chain reaction microchip fabricated in polycarbonate

This paper presents a novel method for DNA thermal amplification using the polymerase chain reaction (PCR) in an electrokinetically driven synchronized continuous flow PCR (EDS-CF-PCR) configuration carried out in a microfabricated polycarbonate (PC) chip. The synchronized format allowed patterning a shorter length microchannel for the PCR compared to nonsynchronized continuous flow formats, permitting the use of smaller applied voltages when the flow is driven electrically and also allowed flexibility in selecting the cycle number without having to change the microchip architecture. A home-built temperature control system was developed to precisely configure three isothermal zones on the chip for denaturing (95 degrees C), annealing (55 degrees C), and extension (72 degrees C) within a single-loop channel. DNA templates were introduced into the PCR reactor, which was filled with the PCR cocktail, by electrokinetic injection. The PCR cocktail consisted of low salt concentrations (KCl) to reduce the current in the EDS-CF-PCR device during cycling. To control the EOF in the PC microchannel to minimize dilution effects as the DNA "plug" was shuttled through the temperature zones, Polybrene was used as a dynamic coating, which resulted in reversal of the EOF. The products generated from 15, 27, 35, and 40 EDS-CF-PCR amplification cycles were collected and analyzed using microchip electrophoresis with LIF detection for fragment sizing. The results showed that the EDS-CF-PCR format produced results similar to that of a conventional block thermal cycler with leveling effects observed for amplicon generation after approximately 25 cycles. To the best of our knowledge, this is the first report of electrokinetically driven synchronized PCR performed on chip.     

Stress Relaxation in Peel Adhesion

The peeling of an adhesive joint consisting of an SBS copolymer and two Mylar film substrates proceeds by cohesive rubber rupture, and the strength increases with test rate. Stress relaxation during peeling is shown to account for this behavior and relaxation data after peeling is used to predict the rate dependence of the peel force.     

Anxiety and cancer treatment: Response to stressful radiotherapy.

Conducted a study with 19 White female cancer patients (aged 23–78 yrs) to document the magnitude of anxiety Ss experienced in response to one particularly stressful form of radiation treatment. In addition, the change in anxiety responses with repeated exposures and individual differences among Ss was explored. As the time for internal radiotherapy treatment neared, subjective and physiologic indicants of anxiety and distress among the Ss significantly increased. By 24 hrs posttreatment, anxiety for all Ss remained elevated. A subset of the Ss who required 2 applications of radiotherapy continued to respond negatively during the 2nd treatment. Data on individual differences in anxiety responses suggest that those with low levels of pretreatment anxiety experienced considerable disruption posttreatment. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Production of pure phosphoric acid from El-Sebaeya low-grade phosphate ore

The extraction of phosphoric acid by tributyl phosphate (TBP) in kerosene from hydrochloric acid leach liquor of El-Sebaeya low-grade phosphate ore was carried out. The influence of various factors affecting the leaching process such as particle size, reaction time, acid concentration, liquid/solid mass ratio, reaction temperature and stirring speed were thoroughly studied to estimate the favor phosphate ore dissolution in relation to impurity. Thereafter, the effects controlling the extraction step, including shaking time, solvent concentration, aqueous/organic phase ratio, and reaction temperature, have been studied in terms of the maximum P₂O₅ extraction efficiency and the minimum impurities extraction efficiency. The obtained loaded organic solvent was subjected to the stripping stage using double-distilled water. The outlet stripping liquor was concentrated by evaporation up to 62% P₂O₅.     

Modeling and closed‐loop control of particle size and initial burst of PLGA biodegradable nanoparticles for targeted drug delivery

An in‐house computer code based on artificial intelligence has been developed and applied in modeling and closed‐loop optimization of release behavior of Poly(lactic‐co‐glycolic acid) (PLGA) biodegradable particles. A series of micro‐ and nanoparticles were prepared via water‐in‐oil‐in‐water double emulsion to be loaded with albumin–fluorescein isothiocyanate conjugate as a typical drug. The interrelationship between input variables (molecular weight of polymer and stabilizer, polymer concentration, and sonication rate) and outputs (PLGA particle size and percentage of initial burst) was uncovered with the aid of artificial neural network modeling. The regression analysis confirmed acceptable correlation coefficients for the aforementioned responses, where the PLGA molecular weight played the most important role among the studied variables. Input variables needed to minimize PLGA size and PLGA initial burst were then obtained via multiobjective optimization performed by a genetic algorithm. PLGA nanoparticles were checked for particle size and particle size distribution using scanning electron micrographs. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45145.     

A comparison between lignin modified by ionic liquids and glyoxalated lignin as modifiers of urea-formaldehyde resin

The aim of this research was to compare the influence of modified lignin by ionic liquid (IL) on the physical and mechanical properties of wood-based panels bonded with urea-formaldehyde (UF) resin with the effect of glyoxalated lignin (GL) on UF properties. For this purpose, soda bagasse lignin was respectively modified by 1-ethyl-3-methylimidazolium acetate ([Emim][OAc]) IL and glyoxal and then the various content of modified lignins (10, 15, and 20%) were added at pH=7 during the UF resin synthesis instead of the second urea . The changes in the structure and thermal properties of lignin, after and before modification with glyoxal and IL, were analyzed by Fourier transform infrared spectrometry (FTIR) and differential scanning calorimetry (DSC). The physicochemical properties of the prepared resins as well as the water absorption, shear strength, and formaldehyde emission of the plywood panels made with these adhesives were measured according to standard methods. According to the FTIR spectra, the content of C=O bond increased in GL while in the IL-treated lignin the content of C–N bond markedly increased. DSC analysis indicated that lignin modified by IL had lower glass transition temperature (T_g) value compared to those modified with glyoxal and unmodified lignin, respectively. The UF resins containing IL-treated lignin exhibit a faster gel time compared to those prepared with GL. Equally, the plywood panels prepared with an IL had lower formaldehyde emission and higher mechanical strength compared to those made from UF resin containing GL. There were no significant differences in dimensional stability of the panels bonded with UFs modified with GL and those with IL-modified lignin.     

Application of polyhedral oligomeric silsesquioxane to the stabilization and performance enhancement of poly(4‐methyl‐2‐pentyne) nanocomposite membranes for natural gas conditioning

The application of octatrimethylsiloxy polyhedral oligomeric silsesquioxane (POSS) nanoparticles was investigated in the fabrication of novel reverse‐selective poly(4‐methyl‐2‐pentyne) (PMP) nanocomposite membranes for the separation of heavier hydrocarbons from methane. Generally, PMP and PMP–fumed silica (FS) nanocomposite membranes suffer severe physical aging with approximately 40% permeation flux reduction over 120 days. A straightforward strategy was introduced to suppress the physical aging of PMP and also to improve the thermal stability without compromising the selectivities and permeabilities through the incorporation of a functionalized POSS–FS binary filler system. Fourier transform infrared spectroscopy and scanning electron microscopy proved productive interactions between the fillers and polymer, with a fair compatibility between them. Thermogravimetric analysis confirmed that the thermal stability of the neat PMP was enhanced by the incorporation of the fillers into the nanocomposites. The addition of POSS and FS led to improved operational performance, such as in the permeability and selectivity, over the neat PMP. The permeation stabilities of the PMP–POSS and PMP–FS–POSS nanocomposite membranes were clearly improved over a long time (120 days). The permeation data indicated that the PMP–3 wt % POSS–20 wt % FS nanocomposite membrane is promising for C₃H₈/N₂ and C₃H₈/CH₄ separation. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45158.