Stress Superposition in High-Strength Glass

The introduction of surface compression via alkali-ion exchange is frequently used to strengthen alkali-containing glass. However, previous investigators found that when starting with high-strength glass, the strength measured after exchange was significantly less than the sum of the residual compression and the starting fracture strength. Results are presented which suggest that the source of this discrepancy is surface damage produced during the heat treatment accompanying the ion-exchange process. Further, when the surface damage was removed by shallow hydrofluoric acid etching, the resulting fracture strength did approximately equal the sum of the residual stress and the high starting strength.     

Diluent effects on carbonate mobility in bisphenol-A polycarbonate in the solid state

The effect of miscible low molecular weight additives on the mobility of the carbonate group in bisphenol-A polycarbonate (BPAPC) has been studied using n.m.r. and dielectric relaxation experiments in the solid state. Proton-enhanced dipolar-decoupled carbon-13 n.m.r. spectra of BPAPC, isotopically enriched at the carbonate position, are obtained without magic-angle sample spinning. The resolved chemical shift anisotropy allows study of nuclear spin relaxation for the carbonate groups in the polymer that have different orientations relative to the static magnetic field in the laboratory frame. The spin-lattice relaxation time in the rotating frame (T_1?) is measured at a motional-probe frequency of 50 kHz for the undiluted polymer and for BPAPC-diluent blends containing either dibutylphthalate or dinitrobiphenyl. The T_1? exhibits some dependence on orientation in all systems studied. In the blend containing dibutylphthalate (DBP), T_1? is decreased by a factor of two for all orientations of the carbonate group. This implies that DBP substantially increases the spectral density of 50 kHz motions in the carbonate region of the polymer at ambient temperature. In contrast, dinitrobiphenyl does not significantly alter the Fourier component of thermal fluctuations at 50 kHz. Dielectric relaxation measurements at 10 kHz reveal that the primary (T_g) and secondary (β) motional processes in BPAPC are affected by low molecular weight additives. An intermediate relaxation process appears in the temperature interval between the glass transition temperature (T_g) and the sub-T_g β-relaxation (T_β) in the polymer-diluent blends. The n.m.r. spin-lattice relaxation rate in the rotating frame, T^?1_1?, correlates well with the relative magnitude of the dielectric dissipation factor (tan δ_ε) between T_g and T_β.     

Advances and future prospects in copper electrowinning

In recent years research on the electrowinning of copper has led to a number of significant advances. These developments include improved mass transfer and higher current density operation through air sparging, reduced anode overvoltage in the conventional cell as a result of cobalt(II) addition to the electrolyte or the use of alternative types of anodes, and the production of high quality cathodes in the electrowinning of copper from solvent extraction strip liquor. The fluidized-bed cathode offers the possibility of continuous electrowinning as well as the direct electrowinning of copper from dilute solutions. The problem of high power consumption may find its solution in the adoption of an alternate anode reaction or in the electrowinning of copper (I) electrolytes. Noteworthy is the development of unique electrowinning cells in conjunction with the hydrometallurgical treatment of copper concentrates. These cells utilize cuprous or ferrous anodic oxidation with the resulting cupric or ferric ions being active lixiviants of sulphide copper minerals. The numerous advances combined with the increasing tonnage of copper being produced by the electrowinning route ensure an interesting and promising future for this process.     

An improved apparatus for oxygen bomb testing

An improved oxygen bomb apparatus has been developed. The increased precision and readability of the continuous pressure recording allows a new method of end-point measurement. It was possible to use smaller test samples than any previously reported. Sample size and oxygen pressure were shown to be relatively unimportant variables. Temperature is the most useful variable for controlling test time. This is preferable over sample dispersion or addition of catalysts in terms of simplifying the procedure. Peroxide formation at the oxygen bomb test end point is three to four times the value at the end point of the Active Oxygen Method. Presented at the AOCS meeting, New Orleans, April 1976. Part I of a series on Evaluation of Antioxidant Performance.     

Aeroelastic tailoring and scaling using Bacterial Foraging Optimisation

Bacterial Foraging Optimisation (BFO) is investigated in an attempt to evaluate its use in solving complex optimisation problems for aeronautical structures. A hybrid variant of BFOA, which incorporates meta-modelling techniques, is also proposed and employed. The efficiency and effectiveness of the methods are tested for tailoring a rectangular composite wing, aiming to maximise the flutter speed and for scaling a joined-wing aircraft, targeting to match aeroelastic responses between the physical prototype and wind tunnel model. The obtained results are compared with those found using a range of other biologically inspired optimisation methods (GA, PSO, ACO), proving that the social foraging behavior of motile bacteria is an effective tool for aeroelastic optimisation.     

Responses to prey chemicals by a lacertid lizard,Podarcis muralis: Prey chemical discrimination and poststrike elevation in tongue-flick rate

The ability to discriminate prey chemicals from control substances and the presence of a poststrike elevation in tongue-flicking (PETF) rate are experimentally demonstrated in the lacertid lizard,Podarcis muralis, The tongue-flick attack score, a composite index of response strength, was significantly higher in response to integumental chemicals from cricket than to cologne or distilled water. The cricket chemicals additionally elicited a significantly greater rate of tongue-flicking and higher proportion of attacks by the lizards than did control stimuli. PETF combined with apparent searching movements strongly suggest the presence of strike-induced chemosensory searching (SICS). Experimental evidence indicates that both PETF and SICS occur in insectivorous representatives of three families of actively foraging autarchoglossan lizards, suggesting their widespread occurrence in such lizards. The adaptive roles of chemosensory behavior in the foraging behavior of P.Muralis are discussed. It is proposed that these lizards may form chemical search images and that PETF and SICS may have been present in the lacertilian ancestors of snakes.     

Fischer-tropsch synthesis on a precipitated iron catalyst: Influence of silica support on product selectivities

The influence of silica support on the α-olefins, internal olefins and branched hydrocarbon selectivities of the gasoline range products of a precipitated iron catalyst in the Fischer-Tropsch synthesis was investigated. Three catalysts with varying silica content and constant promoter content were studied. It was found that there is a linear relationship between the silica content of the catalysts and the internal olefin and branched hydrocarbon product selectivities. The selectivities of the aromatic and alcohol products remain relatively constant, indicating that the production of these two groups of compounds is not affected by the presence of silica support in the catalysts.     

—Review Paper—Current State-Of-The-Art Measurements Of Ozone In The Gas Phase And In Solution

This paper is a critical review and summary of the analytical procedures currently used by operating water utilities to control ozone treatment processes, considering disinfection as well as the many oxidative applications of ozone in water treatment applications. The role of common interferences in the various methods is described.

In operating U S., Canadian, European, and Japanese water treatment plants currently employing ozone as a primary disinfectant, ozone nearly always is followed by the addition of small quantities of chlorine, chlorine dioxide, or chloramine to provide the residual in the distribution system and to act as a secondary disinfectant. Clearly, the analytical procedures used must distinguish between the various species. This review critically presents these various factors and their implication with respect to “true values” of ozone determined under widely varying conditions.     

Morphology and properties of poly(vinyl chloride)–polyurethane blends

The objective of this research was to study the morphology and properties of PVC–polyurethane blends. Studies on blends of a segmented polyether polyurethane with PVC were carried out utilizing differential scanning calorimetry, Rheovibron, stress–strain, infrared peak position studies, and infrared dichroism experiments. This thermodynamically incompatible system was made kinetically compatible by precipitation from tetrahydrofuran (THF) solutions. THF–dioxane solution casting and melt processing produced an incompatible system. The compatible polyurethane–PVC system contains a well-mixed PVC–polyether matrix phase as evidenced by T_g shifts, orientation characteristics, and infrared peak position changes. The aromatic urethane segments which exhibit microphase separation in the pure polyurethane are not solubilized by blending with PVC by any of sample preparation methods used in this study.