A new dynamic hydrogen reference electrode for applications in thin-film sensor systems

The realization and applicability of a new dynamic hydrogen reference electrode (DHRE) within an electrochemical microcell for sensor applications is reported. The electrodes are fabricated in thin-film technology and fixed within a flow-through device. An experimental setup for accurate electrochemical potential measurements is described. Smooth platinum, platinized platinum and pHEMA coated electrodes are investigated with regard to their initialization behavior, stability, reproducibility and interference with electrolytes. It is found that platinized platinum DHREs show excellent stability and reproducibility. For uncoated electrodes, the electrochemical potential is established within seconds. The potential is independent of the pH value within the range of pH 4–10. Interference with sulfate and phosphate is observed. Thus, the platinized platinum DHRE is well suited for bioanalytical sensor applications, where the pH value is buffered and the concentrations of the disturbing anions are constant or very low.     

Study of transmission response of edge filters employed in wavelength measurements

The ratiometric wavelength-measurement system is modeled and an optimal design of transmission response of the employed edge filter is demonstrated in the context of a limited signal-to-noise ratio of the signal source. The corresponding experimental investigation is presented. The impact of the limited signal-to-noise ratio of the signal source on determining the optimal transmission response of edge filters for a wavelength-measurement application is shown theoretically and experimentally.     

Description of Structural Damage Caused by the Terrorist Attack on the Pentagon

On September 11, 2001, an airliner was intentionally crashed into the Pentagon. It struck at the first elevated slab on the west wall, and slid approximately 310?ft (94.5?m) diagonally into the building. The force of the collision demolished numerous columns and the fa?ade of the exterior wall, and induced damage to first-floor columns and the first elevated slab over an area approximately 90?ft (27.4?m) wide and 310?ft (94.5?m) long. None of the building collapsed immediately. The portion that remained standing, even after an intense fire, sustained substantial damage at the first-floor level.     

Mass-Balance Model of Pulmonary Oxygen Transport

A dynamic lumped-parameter model for pulmonary gas transport has been developed to characterize the lung and predict the effect of various parameter changes. The gas side of the lung is modeled as a series and parallel arrangement of five perfectly mixed, variable-volume compartments that correspond roughly to airway and alveolar regions. The blood side of the lung is modeled as a series of perfectly mixed, constant-volume compartments that represent the pulmonary capillary bed. From nonsteady mass balances, equations are derived which yield the time course of concentration for each compartment. Model simulations indicate that the oxygen-hemoglobin reaction does not reach equilibrium in the pulmonary capillaries, an assumption commonly made in analyses of pulmonary oxygen transport. Simulations also show the extent to which breathing amplitude and rate can affect the oxygen level in the blood leaving the lung. A comparison of simulations for a normal state and chronic obstructive lung disease (COLD) with identical input conditions demonstrates that the oxygen level in the blood leaving the lung is much lower in COLD. Also, the simulations are compared with experimental findings.     

Investigation of the high-temperature behaviour of coal ash in reducing and oxidizing atmospheres

The high-temperature behaviour of ashes from a suite of coals exhibiting a wide range of mineralogies has been investigated. Phase analysis of ash samples quenched from various temperatures under either a reducing (60% CO/40% CO₂) or an oxidizing (air) atmosphere was performed by Mössbauer spectroscopy, scanning electron microscopy (SEM)/automatic image analysis (AIA), and X-ray diffraction (XRD). It was found that significant partial melting of the ashes occurred at temperatures as low as 200–400 °C below the initial deformation temperature (IDT) defined by the ASTM ash cone fusion test. Melting was greatly accelerated under reducing conditions, for which the percentage of melted ash increased rapidly between 900 and 1100 °C, saturating at temperatures above ≈ 1200 °C. The observation of such phases as wustite (FeO), fayalite (Fe₂SiO₄), hercynite (FeAl₂O₄), and ferrous glass in samples quenched from 900 to 1200 °C indicates that ash melting in a reducing atmosphere is usually controlled by the iron-rich corner of the FeO-Al₂O₃-SiO₂ phase diagram. Ashes rich in CaS are an exception to this rule, for large quantities of iron sulphide are formed and the melting behaviour is controlled in part by the FeO-FeS phase diagram. Under oxidizing conditions, potassium appears to be the most important low-temperature fluxing element, as the percentage of glass in samples quenched from temperatures below 1100 to 1200 °C was proportional to the amount of the potassium-bearing mineral illite contained in the coal. Above 1200 °C in air, calcium and, to a lesser extent, iron became effective as fluxing elements; melting accelerated between 1200 and 1400 °C, and was near completion between 1400 and 1500 °C for most ashes. To retard ash melting, it is generally concluded that aluminium is the most desirable constituent of ash, whereas the most undesirable constituents are iron, calcium, and potassium.     

Physicochemical and morphological properties of poly(aniline-co-pyrrole)

Copolymers of aniline and pyrrole have been prepared by chemical oxidative-polymerization of aniline and pyrrole using ammonium per sulphate and ferric chloride as oxidants. The structural and morphological properties were studied by X-ray diffraction and scanning electron microscopy. Both copolymers showed an amorphous behaviour compared to their homopolymers. SEM micrographs of poly(aniline–pyrrole) copolymer showed agglomerated spherical structures where as poly(2,5-dimethoxyaniline-pyrrole) showed disordered structures of spherical agglomerates. The copolymers showed improved UV–Vis absorption with the broad peak from 450 to 850 nm. The copolymers exhibited a lower conductivity compared to the homopolymers due to the unsuccessful complex between PANI and PPy, induced by the use of APS as the oxidant.     

Rheological characterization of filled polyamide 11 and polyamide 12 solutions in polyols

A thorough understanding of the rheological properties of real-world, formulated polymer melts and solutions is important to fabricate articles via typical melt processing techniques. Polyamides have been studied extensively in the area of water purification applications. In this work, the viscosity of these homogeneous polyamide 11 and polyamide 12 solutions in specific polyols was measured in the single phase region as a function of shear rate and temperature via capillary rheometry. In addition, the viscosity of the same polyamide solutions containing various levels of dispersed, nanoscale calcium carbonate particles was characterized in order to understand the rheology of the filled systems. Viscosity-reduced shear rate master curves were constructed by applying the principle of time–temperature superposition, and the activation energies were measured for the polyamide-polyol solutions. The observed increase in viscosity caused by the addition of nanofiller could not be explained by simply applying a vertical shift to the master curve, and a density exponent was required to account for the stiffening mechanism. Also, the dependence of the relative viscosity on the filler loading was shown to be consistent with the hypothesis that the filler particles were organized in the form of small fractal aggregates. The filled polyamide 11 systems exhibited higher relative viscosities than the filled polyamide 12 systems, indicating a higher level of particle aggregation and larger mean cluster size for the filled polyamide 11 systems. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 48244.