Corrosion of metals and alloys in mixed gas environments at elevated temperatures

The attack of nickel, cobalt, iron, and alloys of these metals containing chromium and aluminum, by gases containing sulfur-oxygen, carbon-oxygen, and nitrogen-oxygen has been studied at temperatures of 600 and 900°C. The degradation of these metals and alloys was characterized by using standard analytical techniques with emphasis on optical metallography. Three types of accelerated degradation were identified for the attack of alloys by gases containing another oxidant in addition to oxygen. One type of degradation occurred because of the formation of reaction products composed of mixtures of phases involving both of the oxidants. Another type resulted from the reaction of second oxidant phases with oxygen. The third form of degradation involved the development of less protective phases due to thermodynamic instabilities. Thermodynamic stability diagrams are used to help account for the effects produced by different elements in the alloys.     

Diffusion in gold and Au-Ag alloys

The self-diffusion coefficients of gold in pure gold and alloys of gold and silver have been measured over a range of temperatures. Chemical interdiffusion coefficients have been measured on pure metal and incremental couples, but are of lower accuracy because of the development of porosity. The results are compared with earlier work and internally on the basis of Darken’s equations.     

Current oscillations in austenitic stainless steel induced by the presence of chloride ions

The conditions for current oscillations in austenitic stainless steel (AISI Type 303) in 1M H₂SO₄ containing Cl^? ions are given. The periodic oscillations are produced in a close potential range determined at the active-passive transition region. It requires a non-homogeneous distribution of inclusions and carbides at the metal surface and a concentration range of Cl^? ion where active and passive areas coexist on the metal surface. The constraints at the surface determining these two regions are related to the Cl^? ion competitive adsorption and the local accumulation of corrosion products. Electrochemical data and SEM observations are correlated.     

Potassium channels: a computer prediction of structure and selectivity

Model structures for the pore of the potassium channels Shakerand ROMK1 are predicted. The models arise from computer simulationsand suggest reasons for the striking selectivity of these channelsfor K+ and the blocking of ROMK1 by internal Mg²⁺. The modelledstructure of the Shaker pore is supported by mutagenesis data.The mutagenesis experiments indicate the side chains responsiblefor binding to blocking agents [tetraethylammonium (TEA) andcharybdotoxin (CTX)] and the model has these side chains suitablyoriented for binding. An aromatic K+ binding site part way downthe pore is also predicted by the Shaker pore model.     

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.     

Electrochemical determination of rusted steel surface stability

The stability of a rusted steel surface exposed to a 0.11 M sodium sulphate solution has been studied. Electrochemical impedance spectroscopy, polarization resistance and atomic absorption analysis techniques were used in conjunction with mild steel specimens rusted in a rural atmosphere and treated with different concentrations of phosphoric acid. Since most of the impedance diagrams obtained differ from the typical semicircle, it is not clear how to obtain kinetic information on the corrosion process. The polarization resistance technique gives more useful data.     

Fine structures and fracture processes in plastic/rubber two -phase polymer systems. I. Observation of fine structures under the electron microscope

Fine structures of several plastic/rubber two -phase polymer systems were studied by means of direct observations of ultrathin sections under the electron microscope using osmium tetroxide staining and a hardening procedure developed recently by Kato. Samples used are several types of both ABS polymers and high -impact polystyrenes, and several PVC/rubber blends and the results were discussed in relation to their dynamic viscoelastic properties. It is suggested that these studies may fruitfully be extended to clarify the structure -to property relationships by use of this method.     

Potentiometric titration of long chain quaternary ammonium compounds using sodium tetraphenyl borate

Current methods for determining the activity of long chain quaternary ammonium compounds (QACS) are based either on dye partition, titration, or colorimetric analysis. The two major disadvantages of these methods are the disparity of partition coefficients among differently constituted QACS and the difficulty in detecting visual end points. Some potentiometric titration methods for QACS have been reported in the literature. However, back titration techniques, as well as complicated electrode systems, are generally involved. A new potentiometric titration system is presented which uses aqueous sodium tetraphenylborate (TPB) solution as a titrant and a platinum-platinum electrode system to detect the end point. Standard potentiometric titration instruments may be used for this method. This new potentiometric method is superior in precision and accuracy to visual (colorimetric) methods. Original version presented at the 1986 Annual AOCS Meeting in Honolulu, HI.     

Factors influencing the formation of elongated morphologies in immiscible polymer blends during melt processing

The morphology of the dispersed phase in immiscible polymer blends plays an important role in the determination of the final physical properties. This paper considers factors that influence the final state of deformation of the dispersed phase, and in particular, the formation of fibers and lamellae. Blends of polyethylene and nylon-6 were extruded by ribbon extrusion at different draw ratios. Prior to single-screw extrusion the materials were blended in a co-rotating twin-screw extruder, and the size of the dispersed phase was studied as a function of the viscosity ratio. As the blends are extruded into ribbons and drawn through the calender rolls, the morphology of the dispersed phase undergoes drastic transformations. The fiber formation is enhanced by increasing the draw ratio. At high draw ratios, long thin fibers are observed. Some biaxial deformation is obtained for the noncompatibilized systems when the extruded materials enter the calender with the maximum closing pressure applied to the rolls. The same effect is observed for the compatibilized systems with lower values of the viscosity ratio. As a general rule, it has been observed that the final dispersed phase deformation is diminished in interfacially compatibilized systems.