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The surface passive film on UNS S30400 alloy was characterized before and after biofilm development under different regimes of diurnal lighting in quiescent flowing coastal seawater. As exemplified by atomic force microscopy, the passive film grew under all test conditions with conspicuous variations in morphological features. X-ray photon spectroscopy illustrated an enrichment of the outer film by iron oxide and a progressive increase in the iron oxide/chromium oxide ratio with lighting. Mott-Schottky plots reflected the duplex nature of the film, comprising an outer n-type and an inner p-type configuration. The slopes of the plots showed a strong decrease in donor and acceptor densities with biofilm coverage and lighting, thus confirming passive film growth. These results provide new insights that passive film enrichment is an intrinsic process under practical marine conditions, and show that the evolution of the passive film is a key step to sustained passivity and/or its breakdown by microbial mechanisms.

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A range of stainless steels, nickel-chromium and nickel-chromium-molybdenum alloys were exposed to coastal seawater from Mandapam (Indian Ocean) and freshwater from a perennial pond. Biofilms from both test waters produced an ennoblement of the open circuit potential (OCP) on all alloys as expected, which was slower but substantially larger in freshwater. In both waters an interesting relationship was perceived between the plateau OCP (Emax) and the mass percentage of the major alloying elements. In particular, iron exhibited strong positive correlations with Emax (r(2) ≥ 0.77; p < 0.0005), while the sum of chromium, nickel and molybdenum presented significant negative correlations (r(2) ≤ -0.81; p = 0.0002). Consistent with the regression analyses, Euclidean distance clustering yielded patterns where Inconel-600 and the nickel-chromium-molybdenum alloys had the smallest similarities of OCP with other alloys. The results emphatically reinforce a key role for surface passive films in the ennoblement phenomenon in natural waters.

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Search for new, cheaper and effective adsorbents especially for textile and leather dye effluents are in constant progress. Batch experiments were carried out for the adsorption of Reactive Black 5 by varying the composition of Sorel Cement. The composition of MgO and MgCl2 are varied. Further the Sorel cement was doped with FeCl3 and its adsorption capacity investigated. The effect of initial dye concentration, pH, and temperature and contact time were studied. The equilibrium data were fitted into Freundlich and Langmuir adsorption isotherms. The adsorption efficiency and adsorption capacity factor were calculated. The composition doped with FeCl3 showed a higher adsorption capacity. Such composites can be used to remove other organic dyes also. The process is chemisorption which increased with temperature and so the rate and extent of adsorption increased. Kinetics studies were fitted into pseudo first order rate expression.

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