Corrosion inhibition in magnesium-aluminium-based alloys induced by rapid solidification processing

The effect of rapid solidification on the corrosion behaviour in aerated 0.001 M NaCl solution of Mg-Al alloys containing 9.6 to 23.4wt% AI has been investigated in comparison with chill-cast material. Polarization studies show that rapid solidification decreases corrosion current by up to two orders of magnitude corresponding to a corrosion rate of 6 to 11 mil y^–1. Increasing the aluminium content in solid solution by rapid solidification gave rise to a steep increase in pitting potential between 10 and 23 wt% Al and resulted in development of an anodic plateau at 30Acm^–2 attributable to magnesium depletion for the alloy surface and formation of a protective film. Chemical analysis of the electrolyte as a function of dissolution time for the rapidly solidified material indicated that initially only magnesium dissolved and that this dissolution of magnesium ceased within 2 to 5 min. The results indicate the formation of an aluminium-enriched interdiffusion zone at the surface underlying a more stable surface oxide than for ingot-processed Mg-Al-based alloys.     

Surface analytical study of the interaction between γ-amino propyl triethoxysilane and E-glass surface

Time-of-flight secondary ion mass spectrometry has been used to study the interaction of -amino propyl triethoxysilane with an E-glass surface. The fragmentation pattern has been interpreted by assigning a series of mass peaks to the structural unit of the poly(aminosiloxane). The composition of the coating is complicated by the presence of polydimethylsiloxane and its copolymers. The highest mass fragment was obtained from the coating exposed by extraction with warm water (697 AMU). The largest molecular fragments would appear to have degrees of polymerization of 6 with differing numbers of silanol groups. On re-extraction with hot water the fragment size decreased. It is postulated that the network chain length of the three-dimensional polymer decreased as the interface was approached. At the glass surface a chemically bound molecular layer could be identified. The full chemical nature of the deposit is complicated by the incorporation of aluminium from the substrate into the coating. It was also possible to confirm that a layer of warm-water soluble oligomers existed at the air interface.     

An Active Feedback System for Stabilizing Visual Images

In normal vision, eye movements cause the image to move on the retina. Special apparatus can stabilize the image on the retina so it cannot move, and vision fades away. Previous methods for stabilizing the image were either optical systems or complex computer-controlled feedback systems. A simpler feedback system is presented which detects eye motion and rotates a mirror through which the target is viewed, to exactly compensate for eye motion. Unlike previous optical systems, this new system has no lenses in either the viewing or the image-forming path to limit the spatial resolution.     

INVESTIGATION OF THE USE OF LASER-DOPPLER VELOCIMETRY IN TWO-PHASE BUBBLY FLOWS

Understanding the dynamic phenomena of viability loss of shear sensitive cells and bubble breakage and coalescence within airlift reactors requires knowledge of local, liquid-phase hydrodynamics. The laser-Doppler velocimeter (LDV) is a non-invasive instrument which may be used to obtain this information. Experimental procedures and software were developed to detect and measure Doppler bursts in two-phase flow in a split-cylinder airlift reactor. Off-line analysis of the data indicated a detection rate approximately one order of magnitude greater than that observed using an available commercial frequency tracker. Approximately 400 to 500 observations are needed for the ensemble mean to characterize the local mean velocity to within ±5% for a superficial gas velocity of 10.4 cm/s, the highest superficial gas velocity used in these studies. The limitations, prospects, and signal-processing options for LDV in this application are also discussed     

An analysis of moving-bed flow of solids down standpipes and side valves

A method of analysing solids downflow through standpipe and slide valve in the moving bed mode is presented. The method is based on combining Yoon and Kunii equations for moving-bed flow with a proposed modified orifice equation for gas—solid flow. The analysis correctly predicts the observed trend of the effects of gas injection into the standpipe. It also provides quantitative prediction of the conditions for transition from moving-bed flow to dense phase fluidized solids flow and to lean phase “streaming flow”. The latter flow pattern refers to solids streaming down a tube at high voidage typified by the discharge of solid down a tube with no constriction at the lower end of the tube. Further work is required to test the general applicability of the present analysis and to extend the analysis to yield a generalized quantitative flow regime diagram for downflow of solids in a pipe.     

Observations on the relatively high strength of a chalk-aggregate concrete

It has been observed that concrete containing chalk aggregate had a higher compressive strength than other wise similar concrete which contained basalt aggregate, although the chalk rock had a lower compressive strength than the basalt. Measurements of the rates of development of hardness of concrete containing these aggregates, measurements of the surface areas of these aggregates and X-ray examinations of the crystal phases in the set cement are reported and discussed. It was concluded that the relatively low strength of concrete containing basalt aggregate may be due to development of a phase, not chemically identified in the present work, which had a relatively weak bonding strength to the augite crystals in the basalt concrete.     

Studies of microhardness and mar resistance using a scanning probe microscope

Scanning probe microscopy (SPM) is in a period of rapid development. It shows great promise for characterizing coating surfaces. This paper describes modification of an SPM so that it can be used to mar the surfaces of coatings under controlled conditions and to characterize the mars. Mar resistance of coatings is analyzed in terms of a ‘three response, two mechanism model.' The three responses (fracture, elastic, and plastic) can be measured quantitatively using the SPM. Of the three responses, only two (fracture and plastic deformation) are marring mechanisms – elastic deformations recover instantaneously. In some cases mars resulting from plastic deformation may recover slowly with time or with immersion in water; this phenomenon is attributed to viscoelastic creep. Microhardness is also measured with the modified SPM. Some thermoset coatings appear to be substantially harder near their surfaces than in the mass of material, and such materials may respond quite differently to stress applied at different levels near the surface. This finding has important implications for all coating properties that are strongly influenced by the surface. A quantity called ‘micro mar resistance' is defined. It may be useful for comparing different coatings under specified conditions of marring. However, there can be no single quantity that expresses ‘mar resistance' of a coating under all conditions.     

Programmed cooling crystallization of potassium sulphate solutions

The crystal size distribution from a batch cooling crystallizer is predicted by the numerical solution of a mathematical model which uses empirical kinetics of nucleation and crystal growth. The predictions clearly point out the potential advantages of controlled cooling at a constant nucleation rate for improving the product crystal size over that obtained by either natural or linear cooling.Experimental runs following programmed cooling curves for seeded potassium sulphate solutions showed reasonable agreement with the theoretical predictions. A size dispersion of the crystals was observed which contributes to a slight deviation from theory. Nevertheless, controlled cooling significantly reduced the quantity of nuclei formed and improved the product crystal size distribution.     

Characterisation of the neutral oil from a low-temperature coal tar

Tar resulting from fluidised-bed, low-temperature carbonisation of coal was treated to yield a neutral oil from which a series of six other samples was extracted. These were examined by proton magnetic resonance (p.m.r.) spectroscopy, low-ionising-voltage (11 eV) mass spectroscopy (m.s.), gel chromatography followed by fluorescent indicator analysis, and cryoscopy. Aliphatic fractions separated chromatographically were also examined by infra-red spectroscopy. Distributions of hydrogen between chemical types were found for the several fractions from 60 MHz p.m.r. spectra and presented in terms of average structural parameters. M.s. analysis indicated negligible cracking of paraffin components, and the average molecular weight of 197 agreed well with cryoscopic determinations. For the carbon ratio, f_a, between aromatic and total, agreement between m.s. and p.m.r. depends on the p.m.r. structural analysis scheme adopted. P.m.r. and m.s. structural analyses of the aromatics emphasise the predominance of di- and tri-nuclears, with about 40% of available sites substituted, and the importance of acenes in lowtemperature carbonisation material. Gas and gel chromatography showed urea-adductable paraffins to be largely straight-chain C₁₀-C₂₆, much as for tars from carbonisation at higher temperature.