Localized corrosion of (lean) duplex stainless steels in immersion units of urban wastewater treatment plants

With lower alloying cost and higher mechanical properties, lean duplex stainless steels can be an alternative to the more commonly used austenitic stainless steels. However, these alloys are still not the preferred choice, probably due to a lack of field experience. A study was thus initiated in view of defining the limits of use of selected (lean) duplexes for urban wastewater treatment units. The present paper shows the localized corrosion performance of selected lean duplexes in chloride contaminated solutions. The results are compared with austenitic S30403 and S31603 and with the more standard duplexes S82441 and S32205. The effect of welding was also investigated. Exposures in field municipal wastewater plants were conducted for 1 year in low and high chloride content units. The results show that lean duplexes S32101 and S32202 can be used as alternatives to S30403 and S31603 in low chloride electrolytes. At 500 ppm of chloride content, duplex stainless steel S32304 showed better corrosion resistance than S30403 and S31603. For higher chloride contents (1000 ppm and above) the standard duplexes S82441 and S32205 shall be preferred.     

Compact LED projector with tapered light pipes for moderate light output applications

LED-based projectors have numerous advantages compared to traditional projectors. They are more compact, exhibit a larger color gamut and a longer lifetime, the supply voltage is lower and they can even operate on batteries. Despite their optical power per étendue is significantly lower than that of an UHP-lamp, they can be used in low power applications.In this paper, we will present a very compact architecture that produces almost 60 lm D65 light with one red, one green and one blue LED and three small LCOS panels (0.64 in.). In this architecture we have replaced the collection lenses, light pipes (or lens arrays) and relay lenses by ‘Gradually Tapered Light Pipes’.     

Testing of electrochromic materials using symmetrical devices

“Symmetric materials” devices, where both electrodes are made of the same electrochromic materials, allow the in situ study of side reactions. Each transferred charge that is not used for the expected electrochromic reaction will cause a colour change in the whole symmetric device. Two electrochromic materials, WO₃ and IrO₂, are successively used to show how to obtain information about side reactions such as faradaic efficiency, reversibility and potential limits from the symmetric experiment. This in situ approach with a polymer electrolyte shows significant differences compared to results obtained with studies in aqueous electrolytes.     

In Situ FTIR Study of the Formation of an Organosilane Layer at the Silica/Solution Interface

An FTIR experiment especially designed to study the growth of an organosilane layer at the interface between a solution and a flat silica surface is presented. High sensitivity is achieved by using the attenuated total reflection (ATR) technique in a liquid flow cell. The ATR crystal, either silicon or germanium, is covered with a very thin silica layer. Chemical reactions of a mono-and a di-hydrolyzable silane with the silica substrate have been investigated. The grafting of a submonolayer of the first reagent has been monitored by following the C-H and SiO-H vibrations. The density of grafted molecules has been estimated and information on the nature of the chemical bonding has been achieved. Evidence for the chain-polymerization of the dihydrolyzable silane at the substrate/solution interface has been inferred from the appearance of a Si-O-Si absorption band.     

Sodium Coordination Environments in Silica Films

The local structure centered on sodium after diffusion in silica (Na-SiO₂ samples) has been determined by means of extended X-ray absorption fine structure (EXAFS) studies. The Na-SiO₂ samples are of particular interest because (i) their sodium content can be varied over a wide range of concentration and (ii) their local structure is representative of that of soda–silica glass. EXAFS analyses reveal the existence of a well-defined local structure involving oxygen, sodium, and silicon neighbors. The Na-O, Na-Na, and Na-Si bonds lengths, which amount to 0.23, 0.30, and 0.38 nm, respectively, do not depend on sodium concentration. This environment closely resembles that found in soda–silica glass. Moreover, it is compatible with the "target site" and "the site memory effect" suggested by recent theories of the ionic conductivity in oxide glasses.     

Electrochemical study of liquid-solid mass transfer in packed bed electrodes with upward and downward co-current gas-liquid flow

Hydrodynamic and mass transfer parameters (pressure drop, gas and liquid hold-up, liquid-solid mass transfer coefficients) have been measured for porous electrodes with upward or downward co-current gas-liquid flow by means of several electrochemical techniques. The influence of the most important parameters (packing diameter, gas and liquid flow rates) and of the hydrodynamic flow regimes, has been studied. It is found that in the trickle flow regime the limiting current densities depend only on the liquid flow rates (with no measurable influence of the gas). In the upward flow configuration, the strong turbulence generated by the ascending gas bubbles leads to a sharp increase of current densities with the gas flow rate. A comparison between both configurations is presented.     

Comparison Between a Pt–Rh/Ba/Al2O3 and a Newly Formulated NOX-Trap Catalysts Under Alternate Lean–Rich Flows

In situ FT-IR spectroscopy coupled with mass spectrometry have been used to study the mechanism of nitrates formation and reduction over a common Pt–Rh/Ba/Al₂O₃ NO _x storage catalyst, compared with a different alumina-based compound.The experimental device used consists of a transmission reactor cell (having a very small dead volume) dedicated to the evolution of surface species, and of a mass spectrometer combined with a FT-IR micro-cell for gas analysis, allowing time resolved analysis in stationary and transient conditions.At the first time the nitration properties of the catalysts under a lean flow have been studied in the appropriate temperature window (473–673 K). The dynamics of nitrates formation has been pointed out, as well as the different coordination sites on the compounds surface. Then the catalysts have been alternatively exposed to rich and lean flows very close to the real exhaust composition. This has allowed the identification of reduction pathway, active sites, intermediate species and by-products for NO _X -trap reaction. In particular, we have differentiated the role of the support and of the noble metal in the mechanism, as well as of isocyanate adspecies and ammonia among the detected species. The very high NO _X storage properties and the selectivity (near 100%) in nitrogen of the newly designed catalyst have been pointed out.     

Sorption of ethene and ethane on the V2O5(001)/TiO2(001) anatase interface

Simulation techniques have been employed to investigate the differences in the low energy adsorption configurations of ethene and ethane on the TiO₂ supported and unsupported V₂O₅(001) surface. We find that the ethene molecule approaches much closer to thesupported V₂O₅(001) surface which is reflected in the 40 kj mol^–1 higher adsorption energy. The low energy adsorption configuration located for ethane on the supported V₂O₅ shows that the molecule does not approach as close to the supported V₂O₅ surface as does ethene, resulting in the adsorption energy of ethane being 52 kJ mol^–1 lower than that of ethene on the supported V₂O₅ surface.     

Role of the nature of the acid sites in the oxydehydrogenation of propane on a VPO/TiO2 catalyst. An in situ FT-IR spectroscopy investigation

Catalytic activity and surface acidity during the oxydehydrogenation of propane over a VPO/TiO₂ catalyst were determined by a dynamic in situ FT-IR spectroscopy technique at 350°C. Pyridine was used as a probe molecule for the acidity measurements. The obtained results show that propene formation is linked to Brønsted acid sites and that water increases the number of these sites which, in turn, increases propene selectivity.     

On the probabilistic-deterministic transition involved in a fragmentation process of brittle materials

Dynamic loadings produce high stress waves leading to the fragmentation of brittle materials such as ceramics, concrete, glass and rocks. The main mechanism used to explain the change of the number of fragments with stress rate is a shielding phenomenon. However, under quasi-static loading conditions, a weakest link hypothesis may be applicable. Therefore, depending on the local strain or stress rate, different fragmentation regimes are observed. One regime corresponds to single fragmentation for which a probabilistic approach is needed. Conversely, the multiple fragmentation regime may be described by a deterministic approach. The transition between the two fragmentation regimes is discussed for high performance concrete, glass and SiC ceramics.