The incidence of OAC in non-dysplastic BO is around 1 per 300 patients per year. The incidence of OAC in short-segment BO is under 1 per 500 patients per year.

Gold and silver nanoparticles can be stabilized endogenously within aquatic environments from dissolved ionic species as a result of mineralization induced by dissolved organic matter. However, the ability of fulvic and humic acids to stabilize bimetallic nanoparticles is entirely unexplored. Elucidating the formation of such particles is imperative given their potential ecological toxicity. Herein, we demonstrate the nucleation, growth, and stabilization of bimetallic Ag-Au nanocrystals from the interactions of Ag and Au with Suwannee River fulvic and humic acids. The mechanisms underpinning the stabilization of Ag-Au alloy NPs at different pH (6.0-9.0) values are studied by UV-vis spectrophotometry, X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HRTEM), and selected area electron diffraction (SAED). Complexation of free Ag and Au ions with the Lewis basic groups (carbonyls, carboxyls, and thiols) of FA and HA, followed by electron-transfer from redox-active moieties present in dissolved organic matter initiates the nucleation of the NPs. Alloy formation and interdiffusion of Au and Ag atoms are further facilitated by a galvanic replacement reaction between AuCl and Ag. Charge-transfer from Au to Ag stabilizes the formed bimetallic NPs. A more pronounced agglomeration of the Ag-Au NPs is observed when HA is used compared to FA as the reducing agent. The bimetallic NPs are stable for greater than four months, which suggests the possible persistence and dispersion of these materials in aquatic environments. The mechanistic ideas have broad generalizability to reductive mineralization processes mediated by dissolved organic matter.

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Abstract:In the present work, erosion wear due to slurry mixture flow has been investigated using a slurry erosion pot tester. Erosion tests are conducted on three different slurry pipe materials, namely, mild steel, SS202, and SS304, to establish the influence of rotational speed, concentration, and time period. In order to increase erosion wear resistance, a high-velocity oxy-fuel (HVOF) coating technique is used to deposit a WC-10 Co 4 Cr coating on the surface of all piping materials. Experimental results show that rotational speed is a highly-influencing parameter for the erosion wear rate as compared to solid concentration, time duration, and weighted mean diameter. WC-10 Co 4 Cr HVOF coating improved the erosion resistance of piping materials up to 3.5 times. From experimental data, the exponents of solid concentration, velocity, and the size of particles are calculated for the empirical erosion wear equation. A functional equation of the erosion wear rate is developed. The predicted erosion wear is in agreement with the experimental data and found to be within a deviation of ±12%.

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